hypertrophic cardiomyopathy 11

Summary

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,

Xenbase Genes Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

: actc1

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0012799 - hypertrophic cardiomyopathy 11

MONDO:0012799 - hypertrophic cardiomyopathy 11

OMIM:

OMIM:612098 - CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 11; CMH11

OMIM: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)