Monarch Disease Ontology identifier MONDO_0011003 (dilated cardiomyopathy 1E) is any familial isolated dilated cardiomyopathy in which the cause of the disease is a mutation in the SCN5A gene. Also known as: CDCD2, CMD1E, SCN5A familial isolated dilated cardiomyopathy, cardiomyopathy dilated with conduction defect type 2, cardiomyopathy, dilated, 1E, cardiomyopathy, dilated, type 1E, cardiomyopathy, dilated, with conduction defect 2, cardiomyopathy, dilated, with conduction disorder and arrhythmia.