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ONTOLOGY REPORT - ANNOTATIONS


Term:dilated cardiomyopathy 1O
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Accession:DOID:0110451 term browser browse the term
Definition:A dilated cardiomyopathy that has_material_basis_in mutation in the ABCC9 gene on chromosome 12p12.1. (DO)
Synonyms:exact_synonym: CMD1O;   Cardiomyopathy, Dilated, with Ventricular Tachycardia
 primary_id: MESH:C563906
 alt_id: OMIM:608569;   RDO:0013039
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dilated cardiomyopathy 1O term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Abcc9 ATP binding cassette subfamily C member 9 JBrowse link 4 176,806,098 176,928,540 RGD:7240710
RGD:8554872

Term paths to the root
Path 1
Term Annotations click to browse term
  disease 15620
    Developmental Diseases 8739
      Congenital, Hereditary, and Neonatal Diseases and Abnormalities 7521
        genetic disease 7009
          monogenic disease 4562
            dilated cardiomyopathy 1O 1
Path 2
Term Annotations click to browse term
  disease 15620
    disease of anatomical entity 14949
      cardiovascular system disease 4286
        heart disease 2379
          cardiomyopathy 931
            intrinsic cardiomyopathy 603
              dilated cardiomyopathy 267
                dilated cardiomyopathy 1O 1
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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.