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Term:dilated cardiomyopathy 1CC
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Accession:DOID:0110424 term browser browse the term
Definition:A dilated cardiomyopathy that has_material_basis_in mutation in the NEXN gene on chromosome 1p31.1. (DO)
Synonyms:exact_synonym: CMD1CC
 primary_id: MESH:C567733
 alt_id: OMIM:613122;   RDO:0015721
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dilated cardiomyopathy 1CC term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Nexn nexilin (F actin binding protein) JBrowse link 2 257,452,937 257,484,607 RGD:7240710

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Path 1
Term Annotations click to browse term
  disease 15984
    disease of anatomical entity 15262
      cardiovascular system disease 4358
        heart disease 2587
          Cardiomegaly 652
            dilated cardiomyopathy 286
              dilated cardiomyopathy 1CC 1
Path 2
Term Annotations click to browse term
  disease 15984
    Developmental Diseases 9281
      Congenital, Hereditary, and Neonatal Diseases and Abnormalities 8095
        genetic disease 7613
          monogenic disease 5382
            autosomal genetic disease 4348
              autosomal dominant disease 2713
                dilated cardiomyopathy 1CC 1
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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.