Term Name: dilated cardiomyopathy 1X
Synonyms: CMD1X, dilated cardiomyopathy with mild or no proximal muscle weakness
Definition: A dilated cardiomyopathy that has_material_basis_in mutation in the FKTN gene on chromosome 9q31.
Ontology: Human Disease [DOID:0110444]   ( DOID:0110444 )

Relationships
is a type of: autosomal recessive disease dilated cardiomyopathy