X-linked dilated cardiomyopathy

Summary

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, dilated cardiomyopathy 3B, DMD-related dilated cardiomyopathy, XLCM

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

: dmd.2, dmd.3, dmd

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0010542 - dilated cardiomyopathy 3B

MONDO:0010542 - dilated cardiomyopathy 3B

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)