hypertrophic cardiomyopathy 10

Summary

DOID:0110316 - hypertrophic cardiomyopathy 10

Disease Ontology Definition:A familial hypertrophic cardiomyopathy that has_material_basis_in mutation in the MYL2 gene.

Synonyms: cardiomyopathy, familial hypertrophic, 10, CMH10

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

: myl2

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0012112 - hypertrophic cardiomyopathy 10

MONDO:0012112 - hypertrophic cardiomyopathy 10

MIM:

MIM:608758 - CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 10; CMH10

MIM:608758 - CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 10; CMH10

Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee

Parent(s): familial hypertrophic cardiomyopathy (is_a), hypertrophic cardiomyopathy (is_a)