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;   RDO:0015157
 alt_id: OMIM:611407
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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

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  disease 14926
    Developmental Diseases 7774
      Congenital, Hereditary, and Neonatal Diseases and Abnormalities 7096
        genetic disease 6457
          dilated cardiomyopathy 1W 2
Path 2
Term Annotations click to browse term
  disease 14926
    disease of anatomical entity 14092
      cardiovascular system disease 4065
        heart disease 2230
          cardiomyopathy 899
            intrinsic cardiomyopathy 567
              dilated cardiomyopathy 270
                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.