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DOID:0111426 - restrictive cardiomyopathy 2
Disease Ontology Definition:A restrictive cardiomyopathy that has_material_basis_in variation in a region on chromosome 10q23.3.
Synonyms: RCM2, familial restrictive cardiomyopathy 2,
Xenbase Genes :
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)