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Summary Literature (0)
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

In OMIM:
OMIM:115197 - CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 4; CMH4

In Mondo Disease Ontology:
MONDO:0007268 - hypertrophic cardiomyopathy 4

Human Disease Resources: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee

Xenbase Genes : mybpc3

Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Parent(s): hypertrophic cardiomyopathy (is_a)