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Human Disease

familial restrictive cardiomyopathy 6

Term ID
DOID:0061025
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. https://pubmed.ncbi.nlm.nih.gov/29357359/
References
Ontology
Human Disease   ( DOID:0061025 )
Relationships
is a type of
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Genes Involved
Zebrafish Models