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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 Bcl2-associated athanogene 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 14759
    Developmental Diseases 7628
      congenital structural myopathy 134
        myofibrillar myopathy 53
          myofibrillar myopathy 6 1
Path 2
Term Annotations click to browse term
  disease 14759
    disease of anatomical entity 13978
      nervous system disease 9097
        peripheral nervous system disease 1998
          neuropathy 1823
            neuromuscular disease 1406
              muscular disease 902
                muscle tissue disease 631
                  myopathy 521
                    congenital structural myopathy 134
                      myofibrillar myopathy 53
                        myofibrillar myopathy 6 1
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