FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
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General Information
Term dilated cardiomyopathy 1E ID (Ontology) DOID:0110433 (Human Disease)
Definition A dilated cardiomyopathy that has_material_basis_in mutation in the SCN5A gene on chromosome 3p22.2.
Also Known As "CDCD2" ; "CMD1E" ; "dilated cardiomyopathy with conduction defect 2" (for all, see Synonyms field below)
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 Genes
 dilated cardiomyopathy 1E       2
 for disease ribbon | dilated cardiomyopathy 1E       2
 model of | dilated cardiomyopathy 1E       2
Spanning Tree (Parents/Children)
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autosomal genetic disease
 |__autosomal dominant disease__
intrinsic cardiomyopathy        |
 |__dilated cardiomyopathy______|
                                dilated cardiomyopathy 1E  2 rec.
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Is a autosomal dominant disease
dilated cardiomyopathy
Part of
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Synonyms
  • "CDCD2" EXACT OMO:0003012
    "CMD1E" EXACT OMO:0003012
    "dilated cardiomyopathy with conduction defect 2" EXACT
    "dilated cardiomyopathy with conduction disorder and arrhythmia" EXACT
Secondary IDs
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ICD10CM:I42.0
MIM:601154