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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: RCM1, familial restrictive cardiomyopathy 1,

Xenbase Genes : 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)