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

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Path 1
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  disease 14926
    Developmental Diseases 7774
      Congenital, Hereditary, and Neonatal Diseases and Abnormalities 7096
        genetic disease 6457
          dilated cardiomyopathy 1B 2
Path 2
Term Annotations click to browse term
  disease 14926
    disease of anatomical entity 14092
      cardiovascular system disease 4065
        heart disease 2230
          cardiomyopathy 899
            intrinsic cardiomyopathy 567
              dilated cardiomyopathy 270
                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.