Term Name: familial restrictive cardiomyopathy 6
Synonyms: RCM6, restrictive cardiomyopathy 6
Definition: A restrictive cardiomyopathy characterized by prenatal onset of severe restrictive cardiomyopathy predominantly involving the right ventricle, resulting in irreversible heart failure and early death that has_material_basis_in compound heterozygous mutation in the KIF20A gene on chromosome 5q31.
Ontology: Human Disease [DOID:0061025]   ( DOID:0061025 )

Relationships
is a type of: autosomal recessive disease restrictive cardiomyopathy