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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;   RDO:9000708
For additional species annotation, visit the Alliance of Genome Resources.


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dilated cardiomyopathy 1KK term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Mybpc3 myosin binding protein C, cardiac JBrowse link 3 79,940,509 79,958,731 RGD:8554872
G Mypn myopalladin JBrowse link 20 26,988,820 27,074,106 RGD:8554872
RGD:7240710

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Path 1
Term Annotations click to browse term
  disease 14924
    Developmental Diseases 7770
      Congenital, Hereditary, and Neonatal Diseases and Abnormalities 7092
        genetic disease 6457
          dilated cardiomyopathy 1KK 2
Path 2
Term Annotations click to browse term
  disease 14924
    disease of anatomical entity 14094
      cardiovascular system disease 4056
        heart disease 2223
          cardiomyopathy 892
            intrinsic cardiomyopathy 558
              dilated cardiomyopathy 263
                dilated cardiomyopathy 1KK 2
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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.