familial hypertrophic cardiomyopathy

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Summary

Literature (0)

DOID:0080326 - familial hypertrophic cardiomyopathy

Disease Ontology Definition:A hypertrophic cardiomyopathy that is characterized by thickening of the heart muscle and has_material_basis_in autosomal dominant inheritance of one or more gene mutations.

Synonyms:

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

: mybpc3, actc1, tnnc1, myl2, tnnt2, tpm1, tnni3, nexn, flnc, myoz2, prkag2, myl3, cav3.1, jph2, myh6, [+]

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

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

Parent(s): hypertrophic cardiomyopathy (is_a)