Term Name: | familial restrictive cardiomyopathy 6 |
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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 ) |