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ONTOLOGY REPORT - ANNOTATIONS


Term:myofibrillar myopathy 6
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Accession:DOID:0080097 term browser browse the term
Definition:A myofibrillar myopathy that has_material_basis_in heterozygous mutation in the BAG3 gene on chromosome 10q26. (DO)
Synonyms:exact_synonym: BAG3-related myofibrillar myopathy;   MFM6
 primary_id: MESH:C567843
 alt_id: OMIM:612954;   RDO:0009733;   RDO:0015757
For additional species annotation, visit the Alliance of Genome Resources.


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myofibrillar myopathy 6 term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Bag3 BAG cochaperone 3 JBrowse link 1 199,941,258 199,965,191 RGD:7240710
RGD:8554872

Term paths to the root
Path 1
Term Annotations click to browse term
  disease 16017
    Developmental Diseases 9307
      congenital structural myopathy 134
        myofibrillar myopathy 54
          myofibrillar myopathy 6 1
Path 2
Term Annotations click to browse term
  disease 16017
    disease of anatomical entity 15273
      nervous system disease 10762
        peripheral nervous system disease 2363
          neuropathy 2179
            neuromuscular disease 1712
              muscular disease 1126
                muscle tissue disease 757
                  myopathy 611
                    congenital structural myopathy 134
                      myofibrillar myopathy 54
                        myofibrillar myopathy 6 1
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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.