has material basis in X-linked monogenic disease dilated cardiomyopathy 3C MIM:301163 A dilated cardiomyopathy that is characterized by severe arrhythmogenic dilated cardiomyopathy (DCM) with onset as young as the teen years but usually in the third to fifth decades of life and that has_material_basis_in mutation in the gene encoding emerin (EMD) on chromosome Xq28. disease_ontology DOID:0051073 dilated cardiomyopathy X-linked inheritance