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ONTOLOGY REPORT - ANNOTATIONS


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 15599
    disease of anatomical entity 14927
      cardiovascular system disease 4229
        heart disease 2342
          Cardiomegaly 623
            dilated cardiomyopathy 265
              dilated cardiomyopathy 1B 2
Path 2
Term Annotations click to browse term
  disease 15599
    Developmental Diseases 8726
      Congenital, Hereditary, and Neonatal Diseases and Abnormalities 7507
        genetic disease 6997
          monogenic disease 4558
            autosomal genetic disease 3509
              autosomal dominant disease 2076
                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.