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Term:dilated cardiomyopathy 1P
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Accession:DOID:0110439 term browser browse the term
Definition:A dilated cardiomyopathy that has_material_basis_in mutation in the PLN gene on chromosome 6q22. (DO)
Synonyms:exact_synonym: CMD1P
 primary_id: MESH:C563690
 alt_id: OMIM:609909;   RDO:0012883
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dilated cardiomyopathy 1P term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Cep85l centrosomal protein 85-like JBrowse link 20 34,574,043 34,743,142 RGD:8554872
G Pln phospholamban JBrowse link 20 34,633,157 34,642,904 RGD:7240710

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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 1P 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 1P 2
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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.