hypertrophic cardiomyopathy 16

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Summary

Literature (0)

DOID:0110322 - hypertrophic cardiomyopathy 16

Disease Ontology Definition:A familial hypertrophic cardiomyopathy that has_material_basis_in heterozygous mutation in the MYOZ2 gene on chromosome 4q26.

Synonyms: cardiomyopathy familial hypertrophic 16, CMH16

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

: myoz2

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0013455 - hypertrophic cardiomyopathy 16

MONDO:0013455 - hypertrophic cardiomyopathy 16

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)