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ONTOLOGY REPORT - ANNOTATIONS


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
RGD:8554872

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Term Annotations click to browse term
  disease 14924
    Developmental Diseases 7770
      Congenital, Hereditary, and Neonatal Diseases and Abnormalities 7092
        genetic disease 6457
          dilated cardiomyopathy 1CC 1
Path 2
Term Annotations click to browse term
  disease 14924
    disease of anatomical entity 14094
      cardiovascular system disease 4056
        heart disease 2223
          cardiomyopathy 892
            intrinsic cardiomyopathy 558
              dilated cardiomyopathy 263
                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.