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ONTOLOGY REPORT - ANNOTATIONS


Term:Inclusion Body Myopathy 3, Autosomal Dominant
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Accession:DOID:9008434 term browser browse the term
Synonyms:exact_synonym: IBM3;   INCLUSION BODY MYOPATHY, DOMINANT;   Inclusion Body Myopathy, Autosomal Dominant;   Inclusion body myopathy 3;   MYOPATHY, PROXIMAL, AND OPHTHALMOPLEGIA;   MYPOP;   Myopathy with Congenital Joint Contractures, Ophthalmoplegia, and Rimmed Vacuoles
 primary_id: MESH:C538330;   MESH:C565311;   RDO:0013985
 alt_id: OMIM:605637;   RDO:0004294
For additional species annotation, visit the Alliance of Genome Resources.


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Inclusion Body Myopathy 3, Autosomal Dominant term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Fancg FA complementation group G JBrowse link 5 58,448,060 58,456,416 RGD:8554872
G Myh2 myosin heavy chain 2 JBrowse link 10 53,711,895 53,738,164 RGD:7240710
RGD:8554872
G Vcp valosin-containing protein JBrowse link 5 58,426,548 58,445,953 RGD:8554872

Term paths to the root
Path 1
Term Annotations click to browse term
  disease 14924
    disease of anatomical entity 14094
      musculoskeletal system disease 3975
        Joint Diseases 1031
          Contracture 39
            Inclusion Body Myopathy 3, Autosomal Dominant 3
Path 2
Term Annotations click to browse term
  disease 14924
    disease of anatomical entity 14094
      nervous system disease 9141
        peripheral nervous system disease 2004
          neuropathy 1820
            neuromuscular disease 1392
              muscular disease 887
                muscle tissue disease 613
                  myopathy 494
                    myositis 65
                      inclusion body myositis 18
                        Inclusion Body Myopathy 3, Autosomal Dominant 3
paths to the root

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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.