FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
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General Information
Term arrhythmogenic right ventricular dysplasia 13 ID (Ontology) DOID:0110084 (Human Disease)
Definition An arrhythmogenic right ventricular dysplasia that has_material_basis_in heterozygous mutation in the CTNNA3 gene on chromosome 10q21.
Also Known As "arrhythmogenic right ventricular cardiomyopathy 13" ; "ARVC13" ; "ARVD13" (for all, see Synonyms field below)
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 Genes
 arrhythmogenic right ventricular dysplasia 13       1
 for disease ribbon | arrhythmogenic right ventricular dysplasia 13       1
 model of | arrhythmogenic right ventricular dysplasia 13       1
Spanning Tree (Parents/Children)
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autosomal genetic disease
 |__autosomal dominant disease_______________________
intrinsic cardiomyopathy                             |
 |__arrhythmogenic right ventricular cardiomyopathy__|
                                                     arrhythmogenic right ventricular dysplasia 13  1 rec.
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Is a arrhythmogenic right ventricular cardiomyopathy
autosomal dominant disease
Part of
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Synonyms
  • "arrhythmogenic right ventricular cardiomyopathy 13" EXACT
    "ARVC13" EXACT OMO:0003012
    "ARVD13" EXACT OMO:0003012
    "familial arrhythmogenic right ventricular dysplasia 13" EXACT
Secondary IDs
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ICD10CM:I42.8
MIM:615616