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ONTOLOGY REPORT - ANNOTATIONS


Term:dilated cardiomyopathy 1KK
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Accession:DOID:0110445 term browser browse the term
Definition:A dilated cardiomyopathy that has_material_basis_in mutation in the MYPN gene on chromosome 10q21. (DO)
Synonyms:exact_synonym: CMD1KK
 narrow_synonym: CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 22;   CARDIOMYOPATHY, FAMILIAL RESTRICTIVE, 4;   CMH22;   RCM4
 primary_id: OMIM:615248
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show annotations for term's descendants       view all columns           Sort by:
 
dilated cardiomyopathy 1KK term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Mypn myopalladin JBrowse link 20 26,988,820 27,074,106 RGD:8554872
RGD:7240710

Term paths to the root
Path 1
Term Annotations click to browse term
  disease 15984
    Developmental Diseases 9281
      Congenital, Hereditary, and Neonatal Diseases and Abnormalities 8095
        genetic disease 7613
          familial hypertrophic cardiomyopathy 89
            dilated cardiomyopathy 1KK 1
Path 2
Term Annotations click to browse term
  disease 15984
    disease of anatomical entity 15262
      cardiovascular system disease 4358
        vascular disease 3318
          artery disease 2278
            aortic disease 567
              aortic valve disease 271
                aortic valve stenosis 251
                  subvalvular aortic stenosis 207
                    hypertrophic cardiomyopathy 206
                      familial hypertrophic cardiomyopathy 89
                        dilated cardiomyopathy 1KK 1
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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.