neuromuscular disease caused by qualitative or quantitative defects of dystrophin familial dilated cardiomyopathy familial isolated dilated cardiomyopathy https://github.com/monarch-initiative/mondo/issues/5114 https://github.com/monarch-initiative/mondo/issues/6740 https://github.com/monarch-initiative/mondo/issues/6751 https://github.com/monarch-initiative/mondo/issues/6877 https://github.com/monarch-initiative/mondo/issues/7693 https://www.malacards.org/card/familial_isolated_dilated_cardiomyopathy icd11.foundation:949016860 familial isolated dilated cardiomyopathy MEDGEN:1826005 A rare familial cardiomyopathy characterized by the dilation of left ventricle and progressively impairing of systolic ventricular function, in the absence of abnormal loading conditions or coronary artery disease sufficient to cause global systolic impairment. The disease may cause heart failure or arrhythmia. The disease is isolated when no additional atypical cardiac or extracardiac manifestations are present. MONDO:0700335 familial or idiopathic dilated cardiomyopathy UMLS:C5679590 Orphanet:154 GARD:0027293