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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
For additional species annotation, visit the Alliance of Genome Resources.


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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

Term paths to the root
Path 1
Term Annotations click to browse term
  disease 15619
    Developmental Diseases 8737
      Congenital, Hereditary, and Neonatal Diseases and Abnormalities 7519
        genetic disease 7008
          monogenic disease 4561
            dilated cardiomyopathy 1W 2
Path 2
Term Annotations click to browse term
  disease 15619
    disease of anatomical entity 14948
      cardiovascular system disease 4277
        heart disease 2368
          cardiomyopathy 931
            intrinsic cardiomyopathy 603
              dilated cardiomyopathy 267
                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.