FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
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General Information
Term dilated cardiomyopathy 1A ID (Ontology) DOID:0110425 (Human Disease)
Definition A dilated cardiomyopathy that has_material_basis_in mutation in the LMNA gene on chromosome 1q21.
Also Known As "CDCD1" ; "dilated cardiomyopathy with conduction defect 1" ; "familial dilated cardiomyopathy with conduction defect due to LMNA mutation"
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Data Class Field Records
Alleles (FBal)  HUMAN_DISEASE_INTERACTIONS       8
Human Disease Models (FBhh)  DOID       1
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Relevant FlyBase reports
 Alleles Genes Human Disease Models
 dilated cardiomyopathy 1A       8      5      1
 ameliorates | dilated cardiomyopathy 1A       3       --       --
 exacerbates | dilated cardiomyopathy 1A       1       --       --
 for disease ribbon | dilated cardiomyopathy 1A       --       2       --
 model of | dilated cardiomyopathy 1A       4      2       --
Spanning Tree (Parents/Children)
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autosomal genetic disease
 |__autosomal dominant disease__
intrinsic cardiomyopathy        |
 |__dilated cardiomyopathy______|
                                dilated cardiomyopathy 1A  14 rec.
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Is a autosomal dominant disease
dilated cardiomyopathy
Part of
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Synonyms
  • "CDCD1" EXACT OMO:0003012
    "dilated cardiomyopathy with conduction defect 1" EXACT
    "familial dilated cardiomyopathy with conduction defect due to LMNA mutation" EXACT
Secondary IDs
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MIM:115200
ORDO:300751