Hereditary inclusion body myopathy

inherited genetic condition resulting in muscle weakness
MedicalCondition disease Q5737853
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Hereditary inclusion body myopathy

Summary

Hereditary inclusion body myopathy is a disease[1].

Key Facts

  • Hereditary inclusion body myopathy's instance of is recorded as disease[2].
  • Hereditary inclusion body myopathy is a type of muscular disease[3].
  • Hereditary inclusion body myopathy is a type of inclusion myopathy[4].

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APA 4ort.xyz Knowledge Graph. (2026). Hereditary inclusion body myopathy. Retrieved May 3, 2026, from https://4ort.xyz/entity/hereditary-inclusion-body-myopathy
MLA “Hereditary inclusion body myopathy.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/hereditary-inclusion-body-myopathy.
BibTeX @misc{4ortxyz_hereditary-inclusion-body-myopathy_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{Hereditary inclusion body myopathy}}, year = {2026}, url = {https://4ort.xyz/entity/hereditary-inclusion-body-myopathy}, note = {Accessed: 2026-05-03}}
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Edit History

Rolling log of changes to this entity's Wikidata record. Values shown reflect the current state of each edited property — follow the history link to see the precise diff for any edit.

  1. 1d ago · JhealdBatch bot · 2026-07-04 view diff on Wikidata ↗
    Imported from
    Wikiprojectmed id Hereditary inclusion body myopathy
    Microsoft academic id (discontinued) 2776823398
    Icd-11 id (foundation) 1248099703
    + 4 other properties edited (see Wikidata diff for full list)
    "/* wbeditentity-update:0| */ QuickStatements 3.0 [[:toollabs:qs-dev/batch/39873|batch #39873]]: P31 = "type of disease""
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