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;   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
RGD:8554872

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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
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  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.