X-linked dilated cardiomyopathy

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Echinobase

Summary

Literature (0)

DOID:0110461 - X-linked dilated cardiomyopathy

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

Synonyms: CMD3B, DMD-related dilated cardiomyopathy, dilated cardiomyopathy 3B, XLCM

Echinobase 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

: dmd

MIM:

MIM:302045 - cardiomyopathy, dilated, 3b; cmd3b

MIM:302045 - cardiomyopathy, dilated, 3b; cmd3b

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)