ONTOLOGY REPORT - ANNOTATIONS


Term:myofibrillar myopathy 4
go back to main search page
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.


show annotations for term's descendants       view all columns           Sort by:
 
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 14926
    Developmental Diseases 7782
      congenital structural myopathy 134
        myofibrillar myopathy 54
          myofibrillar myopathy 4 1
Path 2
Term Annotations click to browse term
  disease 14926
    disease of anatomical entity 14096
      nervous system disease 9148
        peripheral nervous system disease 2022
          neuropathy 1841
            neuromuscular disease 1417
              muscular disease 914
                muscle tissue disease 636
                  myopathy 525
                    congenital structural myopathy 134
                      myofibrillar myopathy 54
                        myofibrillar myopathy 4 1
paths to the root

NHLBI Logo

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