inclusion body myositis

inflammatory muscle disease in older adults
MedicalCondition designated_intractable_rare_disease Q1848471
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inclusion body myositis

Summary

inclusion body myositis is a designated intractable/rare disease[1]. It has Wikipedia articles in 11 language editions, a strong signal of global cultural recognition.[2]

Key Facts

  • inclusion body myositis's instance of is recorded as designated intractable/rare disease[3].
  • inclusion body myositis's instance of is recorded as rare disease[4].
  • inclusion body myositis's instance of is recorded as class of disease[5].
  • inclusion body myositis is a type of myositis[6].
  • inclusion body myositis is a type of disease[7].
  • inclusion body myositis's symptoms and signs is recorded as muscle weakness[8].
  • inclusion body myositis's symptoms and signs is recorded as muscle atrophy[9].
  • inclusion body myositis's symptoms and signs is recorded as dysphagia[10].
  • inclusion body myositis's has cause is recorded as unknown[11].
  • inclusion body myositis's medical examination is recorded as muscle biopsy[12].
  • inclusion body myositis's medical examination is recorded as creatine kinase measurement[13].
  • inclusion body myositis's medical examination is recorded as electromyography[14].
  • inclusion body myositis's possible treatment is recorded as physiotherapy[15].
  • inclusion body myositis's possible treatment is recorded as speech therapy[16].
  • inclusion body myositis's possible treatment is recorded as artificial nutrition[17].
  • inclusion body myositis's prevalence is recorded as {'amount': '+0.000033'}[18].
  • inclusion body myositis's external data available at URL is recorded as http://www.nanbyou.or.jp/entry/3801[19].
  • inclusion body myositis's ICD-9-CM is recorded as 359.71[20].
  • inclusion body myositis's NCI Thesaurus ID is recorded as C176900[21].
  • inclusion body myositis's health specialty is recorded as rheumatology[22].
  • inclusion body myositis's health specialty is recorded as neurology[23].
  • inclusion body myositis's genetic association is recorded as GNE[24].
  • inclusion body myositis's genetic association is recorded as MYH2[25].
  • inclusion body myositis's exact match is recorded as http://purl.obolibrary.org/obo/DOID_3429[26].
  • inclusion body myositis's exact match is recorded as http://identifiers.org/doid/DOID:3429[27].

Why It Matters

inclusion body myositis has Wikipedia articles in 11 language editions, a strong signal of global cultural recognition.[2] It is known by 21 alternative names across languages and contexts.[28]

References

Programmatic citations — every numbered marker resolves to a verifiable graph row below.

Direct Wikidata claims

  1. [3] . ddrare.nibiohn.go.jp. Retrieved . ddrare.nibiohn.go.jp. Provenance: wikidata.org.
  2. [4] . wikidata.org.
  3. [5] . wikidata.org.
  4. [6] . Disease Ontology. Retrieved . wikidata.org.
  5. [7] . wikidata.org.
  6. [8] . Klinická neurologie část speciální. wikidata.org.
  7. [9] . Klinická neurologie část speciální. wikidata.org.
  8. [10] . Klinická neurologie část speciální. wikidata.org.
  9. [11] . Klinická neurologie část speciální. wikidata.org.
  10. [12] . Klinická neurologie část speciální. wikidata.org.
  11. [13] . Klinická neurologie část speciální. wikidata.org.
  12. [14] . Klinická neurologie část speciální. wikidata.org.
  13. [15] . uptodate.com. Retrieved . uptodate.com. Provenance: wikidata.org.
  14. [16] . uptodate.com. Retrieved . uptodate.com. Provenance: wikidata.org.
  15. [17] . uptodate.com. Retrieved . uptodate.com. Provenance: wikidata.org.
  16. [18] . Q180686. wikidata.org.
  17. [19] . ddrare.nibiohn.go.jp. Retrieved . ddrare.nibiohn.go.jp. Provenance: wikidata.org.
  18. [20] . Disease Ontology. Retrieved . wikidata.org.
  19. [21] . wikidata.org.
  20. [22] . Q180686. wikidata.org.
  21. [23] . Klinická neurologie část speciální. wikidata.org.
  22. [24] . The UDP-N-acetylglucosamine 2-epimerase/N-acetylmannosamine kinase gene is mutated in recessive hereditary inclusion body myopathy. wikidata.org.
  23. [25] . Autosomal dominant myopathy: missense mutation (Glu-706 --> Lys) in the myosin heavy chain IIa gene. wikidata.org.
  24. [26] . Disease Ontology. Retrieved . wikidata.org.
  25. [27] . Identifiers.org. registry.identifiers.org. Provenance: wikidata.org.

Class ancestry

  1. [1] . Wikidata. wikidata.org.

Aggregate / graph-position facts

  1. [2] . Wikidata sitelinks. wikidata.org.
  2. [28] . Wikidata aliases. wikidata.org.

📑 Cite this page

Use these citations when quoting this entity in research, articles, AI prompts, or wherever provenance matters. We aggregate Wikidata + Wikipedia + authoritative open-data sources; the stitched, scored, cross-referenced view is what 4ort.xyz contributes.

APA 4ort.xyz Knowledge Graph. (2026). inclusion body myositis. Retrieved May 3, 2026, from https://4ort.xyz/entity/inclusion-body-myositis
MLA “inclusion body myositis.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/inclusion-body-myositis.
BibTeX @misc{4ortxyz_inclusion-body-myositis_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{inclusion body myositis}}, year = {2026}, url = {https://4ort.xyz/entity/inclusion-body-myositis}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): inclusion body myositis — https://4ort.xyz/entity/inclusion-body-myositis (retrieved 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. 27d ago · JhealdBatch bot · 2026-07-03 view diff on Wikidata ↗
    Subclass of myositis, disease
    Possible treatment physiotherapy, speech therapy, artificial nutrition
    Health specialty rheumatology, neurology
    Medical examination muscle biopsy, creatine kinase measurement, electromyography
    + 9 other properties edited (see Wikidata diff for full list)
    "/* wbeditentity-update:0| */ QuickStatements 3.0 [[:toollabs:qs-dev/batch/39732|batch #39732]]: rm redundant subclass"
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