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Summary Literature (0)
DOID:0110461 - X-linked dilated cardiomyopathy

Disease Ontology Definition:A dilated cardiomyopathy that has_material_basis_in mutation in the gene encoding dystrophin (DMD) on chromosome Xp21, without skeletal muscle weakness or wasting.

Synonyms: CMD3B, DMD-related dilated cardiomyopathy

Xenbase Genes : dmd.2, dmd, dmd

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0010542 - dilated cardiomyopathy 3B


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

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): dilated cardiomyopathy (is_a), X-linked monogenic disease (is_a)