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ONTOLOGY REPORT - ANNOTATIONS


Term:dilated cardiomyopathy 1FF
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Accession:DOID:0110459 term browser browse the term
Definition:A dilated cardiomyopathy that has_material_basis_in mutation in the TNNI3 gene on chromosome 19q13.42. (DO)
Synonyms:exact_synonym: CMD1FF
 primary_id: MESH:C567654
 alt_id: OMIM:613286;   RDO:0015670
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dilated cardiomyopathy 1FF term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Klf5 Kruppel-like factor 5 JBrowse link 15 83,703,796 83,722,921 RGD:8554872
G Tnni3 troponin I3, cardiac type JBrowse link 1 72,882,806 72,886,490 RGD:7240710
RGD:8554872

Term paths to the root
Path 1
Term Annotations click to browse term
  disease 16022
    Developmental Diseases 9336
      Congenital, Hereditary, and Neonatal Diseases and Abnormalities 8164
        genetic disease 7688
          monogenic disease 5446
            dilated cardiomyopathy 1FF 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 1FF 2
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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.