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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.


show annotations for term's descendants       view all columns           Sort by:
 
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 15553
    disease of anatomical entity 14837
      musculoskeletal system disease 4326
        Joint Diseases 1095
          Contracture 58
            Inclusion Body Myopathy 3, Autosomal Dominant 3
Path 2
Term Annotations click to browse term
  disease 15553
    disease of anatomical entity 14837
      nervous system disease 10167
        peripheral nervous system disease 2164
          neuropathy 1988
            neuromuscular disease 1559
              muscular disease 1002
                muscle tissue disease 695
                  myopathy 559
                    myositis 66
                      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.