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ONTOLOGY REPORT - ANNOTATIONS


Term:dilated cardiomyopathy 1W
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Accession:DOID:0110446 term browser browse the term
Definition:A dilated cardiomyopathy that has_material_basis_in mutation in the VCL gene on chromosome 10q22.2. (DO)
Synonyms:exact_synonym: CMD1W
 primary_id: MESH:C566954
 alt_id: OMIM:611407;   RDO:0015157
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dilated cardiomyopathy 1W term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Ap3m1 adaptor related protein complex 3 subunit mu 1 JBrowse link 15 3,435,998 3,454,281 RGD:8554872
G Vcl vinculin JBrowse link 15 3,455,211 3,544,738 RGD:7240710
RGD:8554872

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Path 1
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  disease 16022
    Developmental Diseases 9336
      Congenital, Hereditary, and Neonatal Diseases and Abnormalities 8164
        genetic disease 7688
          monogenic disease 5446
            dilated cardiomyopathy 1W 2
Path 2
Term Annotations click to browse term
  disease 16022
    disease of anatomical entity 15275
      cardiovascular system disease 4377
        heart disease 2600
          cardiomyopathy 1043
            intrinsic cardiomyopathy 707
              dilated cardiomyopathy 286
                dilated cardiomyopathy 1W 2
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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.