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ONTOLOGY REPORT - ANNOTATIONS
Term:nemaline myopathy 11
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Accession:DOID:0110933 term browser browse the term
Definition:An autosomal recessive congenital myopathy characterized by onset of slowly progressive muscle weakness in the first decade, followed by gait difficulties due to proximal muscle weakness and atrophy mainly affecting the lower limbs and neck. Muscle biopsy shows nemaline bodies. (OMIM)
Synonyms:exact_synonym: NEM11;   nemaline myopathy 11, autosomal recessive
 primary_id: OMIM:617336
 alt_id: RDO:9001717
For additional species annotation, visit the Alliance of Genome Resources.

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nemaline myopathy 11 term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Mypn myopalladin JBrowse link 20 26,988,820 27,074,106 RGD:8554872
RGD:7240710
Term paths to the root
Path 1
Term Annotations click to browse term
  disease 15590
    Developmental Diseases 8723
      congenital structural myopathy 129
        nemaline myopathy 56
          nemaline myopathy 11 1
Path 2
Term Annotations click to browse term
  disease 15590
    disease of anatomical entity 14919
      nervous system disease 10196
        peripheral nervous system disease 2111
          neuropathy 1933
            neuromuscular disease 1504
              muscular disease 941
                muscle tissue disease 667
                  myopathy 546
                    congenital structural myopathy 129
                      nemaline myopathy 56
                        nemaline myopathy 11 1
paths to the root

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