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ONTOLOGY REPORT - ANNOTATIONS


Term:myofibrillar myopathy 4
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Accession:DOID:0080095 term browser browse the term
Definition:A myofibrillar myopathy that has_material_basis_in heterozygous mutation in the ZASP gene on chromosome 10. (DO)
Synonyms:exact_synonym: MFM4;   zaspopathy
 primary_id: OMIM:609452
 alt_id: RDO:0009319
For additional species annotation, visit the Alliance of Genome Resources.


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myofibrillar myopathy 4 term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Ldb3 LIM domain binding 3 JBrowse link 16 10,878,348 10,943,016 RGD:7240710
RGD:8554872

Term paths to the root
Path 1
Term Annotations click to browse term
  disease 15625
    Developmental Diseases 8759
      congenital structural myopathy 129
        myofibrillar myopathy 54
          myofibrillar myopathy 4 1
Path 2
Term Annotations click to browse term
  disease 15625
    disease of anatomical entity 14954
      nervous system disease 10224
        peripheral nervous system disease 2126
          neuropathy 1949
            neuromuscular disease 1521
              muscular disease 958
                muscle tissue disease 685
                  myopathy 551
                    congenital structural myopathy 129
                      myofibrillar myopathy 54
                        myofibrillar myopathy 4 1
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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.