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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,
Echinobase Genes : dmd
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):
X-linked disease (is_a),
dilated cardiomyopathy (is_a)