Mondo Description Any familial isolated dilated cardiomyopathy in which the cause of the disease is a mutation in the LAMA4 gene.

Uniprot Description A disorder characterized by ventricular dilation and impaired systolic function, resulting in congestive heart failure and arrhythmia. Patients are at risk of premature death.

Disease Ontology Description A dilated cardiomyopathy that has_material_basis_in mutation in the LAMA4 gene on chromosome 6q21.