restrictive cardiomyopathy 1

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Summary

Literature (0)

DOID:0111425 - restrictive cardiomyopathy 1

Disease Ontology Definition:A restrictive cardiomyopathy that has_material_basis_in heterozygous mutation in the TNNI3 gene on chromosome 19q13.42.

Synonyms: familial restrictive cardiomyopathy 1, RCM1

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

: tnni3

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)