FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
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General Information
Term dilated cardiomyopathy 1J ID (Ontology) DOID:0110440 (Human Disease)
Definition A dilated cardiomyopathy that has_material_basis_in mutation in the EYA4 gene on chromosome 6q23.2.
Also Known As "autosomal dominant dilated cardiomyopathy with sensorineural hearing loss" ; "CMD1J" ; "neurosensory deafness with dilated cardiomyopathy" (for all, see Synonyms field below)
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 Genes
 dilated cardiomyopathy 1J       1
 for disease ribbon | dilated cardiomyopathy 1J       1
 model of | dilated cardiomyopathy 1J       1
Spanning Tree (Parents/Children)
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intrinsic cardiomyopathy
 |__dilated cardiomyopathy__
genetic disease             |
 |__monogenic disease_______|
                            dilated cardiomyopathy 1J  1 rec.
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Is a monogenic disease
dilated cardiomyopathy
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Synonyms
  • "autosomal dominant dilated cardiomyopathy with sensorineural hearing loss" EXACT
    "CMD1J" EXACT OMO:0003012
    "neurosensory deafness with dilated cardiomyopathy" EXACT
    "neurosensory hearing loss with dilated cardiomyopathy" EXACT
    "sensorineural deafness with dilated cardiomyopathy" EXACT
    "sensorineural hearing loss with dilated cardiomyopathy" EXACT
Secondary IDs
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MIM:605362
ORDO:217622