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Term:dilated cardiomyopathy 1B
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Accession:DOID:0110443 term browser browse the term
Definition:A dilated cardiomyopathy that has_material_basis_in variation in the chromosome region 9q13. (DO)
Synonyms:exact_synonym: CMD1B;   CMPD1;   FDC1;   familial dilated cardiomyopathy 1;   familial hypokinetic dilated cardiomyopathy
 primary_id: MESH:C536231
 alt_id: OMIM:600884;   RDO:0001723
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dilated cardiomyopathy 1B term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Fktn fukutin JBrowse link 5 70,522,001 70,578,270 RGD:11576324
G Ttn titin JBrowse link 3 63,565,160 63,837,815 RGD:11554173

Term paths to the root
Path 1
Term Annotations click to browse term
  disease 15984
    disease of anatomical entity 15262
      cardiovascular system disease 4358
        heart disease 2587
          Cardiomegaly 652
            dilated cardiomyopathy 286
              dilated cardiomyopathy 1B 2
Path 2
Term Annotations click to browse term
  disease 15984
    Developmental Diseases 9281
      Congenital, Hereditary, and Neonatal Diseases and Abnormalities 8095
        genetic disease 7613
          monogenic disease 5382
            autosomal genetic disease 4348
              autosomal dominant disease 2713
                dilated cardiomyopathy 1B 2
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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.