FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
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General Information
Term familial restrictive cardiomyopathy 6 ID (Ontology) DOID:0061025 (Human Disease)
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.
Also Known As "RCM6" ; "restrictive cardiomyopathy 6"
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 Genes
 familial restrictive cardiomyopathy 6       1
 for disease ribbon | familial restrictive cardiomyopathy 6       1
 model of | familial restrictive cardiomyopathy 6       1
Spanning Tree (Parents/Children)
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autosomal genetic disease
 |__autosomal recessive disease__
intrinsic cardiomyopathy         |
 |__restrictive cardiomyopathy___|
                                 familial restrictive cardiomyopathy 6  1 rec.
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Is a autosomal recessive disease
restrictive cardiomyopathy
Part of
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Synonyms
  • "RCM6" EXACT OMO:0003012
    "restrictive cardiomyopathy 6" EXACT
Secondary IDs
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MIM:619433