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Term:dilated cardiomyopathy 1G
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Accession:DOID:0110430 term browser browse the term
Definition:A dilated cardiomyopathy that has_material_basis_in mutation in the TTN gene on chromosome 2q31. (DO)
Synonyms:exact_synonym: CMD1G
 primary_id: MESH:C565824
 alt_id: OMIM:604145;   RDO:0014362
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dilated cardiomyopathy 1G term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G PLEKHA3 pleckstrin homology domain containing A3 JBrowse link 2 178,480,454 178,516,463 RGD:8554872
G TTN titin JBrowse link 2 178,525,989 178,807,423 RGD:8554872
G TTN-AS1 TTN antisense RNA 1 JBrowse link 2 178,522,827 178,620,217 RGD:8554872

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Path 1
Term Annotations click to browse term
  disease 16990
    Developmental Diseases 10857
      Congenital, Hereditary, and Neonatal Diseases and Abnormalities 9018
        genetic disease 8514
          monogenic disease 5944
            dilated cardiomyopathy 1G 3
Path 2
Term Annotations click to browse term
  disease 16990
    disease of anatomical entity 16013
      cardiovascular system disease 3680
        heart disease 2619
          cardiomyopathy 1094
            intrinsic cardiomyopathy 753
              dilated cardiomyopathy 309
                dilated cardiomyopathy 1G 3
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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.