restrictive cardiomyopathy 3

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Summary

Literature (0)

DOID:0111427 - restrictive cardiomyopathy 3

Disease Ontology Definition:A restrictive cardiomyopathy that has_material_basis_in heterozygous mutation in the TNNT2 gene on chromosome 1q32.1.

Synonyms: familial restrictive cardiomyopathy 3, RCM3

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

: tnnt2

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

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

Parent(s): restrictive cardiomyopathy (is_a)