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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 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 15619
    Developmental Diseases 8737
      Congenital, Hereditary, and Neonatal Diseases and Abnormalities 7519
        genetic disease 7008
          monogenic disease 4561
            dilated cardiomyopathy 1FF 1
Path 2
Term Annotations click to browse term
  disease 15619
    disease of anatomical entity 14948
      cardiovascular system disease 4277
        heart disease 2368
          cardiomyopathy 931
            intrinsic cardiomyopathy 603
              dilated cardiomyopathy 267
                dilated cardiomyopathy 1FF 1
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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.