Term Name: dilated cardiomyopathy 1E
Synonyms: CDCD2, CMD1E, dilated cardiomyopathy with conduction defect 2, dilated cardiomyopathy with conduction disorder and arrhythmia
Definition: A dilated cardiomyopathy that has_material_basis_in mutation in the SCN5A gene on chromosome 3p22.2.
Ontology: Human Disease [DOID:0110433]   ( DOID:0110433 )

Relationships
is a type of: autosomal dominant disease dilated cardiomyopathy