progressive supranuclear palsy

neurodegenerative disease characterized by supranuclear gaze palsy, postural instability, progressive rigidity, and mild dementia
MedicalCondition designated_intractable_rare_disease Q945930
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progressive supranuclear palsy

Summary

progressive supranuclear palsy is a designated intractable/rare disease[1]. It draws 7,813 Wikipedia views per month (designated_intractable_rare_disease category, ranking #25 of 201).[2]

Key Facts

  • progressive supranuclear palsy's instance of is recorded as designated intractable/rare disease[3].
  • progressive supranuclear palsy's instance of is recorded as rare disease[4].
  • progressive supranuclear palsy's instance of is recorded as class of disease[5].
  • John C. Steele is named after progressive supranuclear palsy[6].
  • Jerzy Olszewski is named after progressive supranuclear palsy[7].
  • progressive supranuclear palsy is a type of movement disorders[8].
  • progressive supranuclear palsy is a type of frontotemporal degeneration with dementia[9].
  • progressive supranuclear palsy is a type of genetic neurodegenerative disease with dementia[10].
  • progressive supranuclear palsy is a type of eye degenerative disease[11].
  • progressive supranuclear palsy is a type of corticobasal degeneration[12].
  • progressive supranuclear palsy is a type of disease[13].
  • progressive supranuclear palsy's Commons category is recorded as Progressive supranuclear palsy[14].
  • progressive supranuclear palsy's external data available at URL is recorded as http://www.nanbyou.or.jp/entry/4114[15].
  • progressive supranuclear palsy's ICD-9-CM is recorded as 333.0[16].
  • progressive supranuclear palsy's NCI Thesaurus ID is recorded as C85028[17].
  • progressive supranuclear palsy's health specialty is recorded as neurology[18].
  • progressive supranuclear palsy's genetic association is recorded as STX6[19].
  • progressive supranuclear palsy's genetic association is recorded as EIF2AK3[20].
  • progressive supranuclear palsy's genetic association is recorded as MOBP[21].
  • progressive supranuclear palsy's genetic association is recorded as MAPT[22].
  • progressive supranuclear palsy's genetic association is recorded as SLCO1A2[23].
  • progressive supranuclear palsy's genetic association is recorded as IRF4[24].
  • progressive supranuclear palsy's genetic association is recorded as CD8B[25].
  • progressive supranuclear palsy's exact match is recorded as http://purl.obolibrary.org/obo/DOID_678[26].
  • progressive supranuclear palsy's exact match is recorded as http://identifiers.org/doid/DOID:678[27].

Why It Matters

progressive supranuclear palsy draws 7,813 Wikipedia views per month (designated_intractable_rare_disease category, ranking #25 of 201).[2] It has Wikipedia articles in 19 language editions, a strong signal of global cultural recognition.[28] It is known by 14 alternative names across languages and contexts.[29]

References

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

Direct Wikidata claims

  1. [3] . mhlw.go.jp. Retrieved . mhlw.go.jp. Provenance: wikidata.org.
  2. [4] . wikidata.org.
  3. [5] . wikidata.org.
  4. [6] . psp.org. psp.org. Provenance: wikidata.org.
  5. [7] . wikidata.org.
  6. [8] . Disease Ontology. Retrieved . wikidata.org.
  7. [9] . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  8. [10] . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  9. [11] . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  10. [12] . wikidata.org.
  11. [13] . wikidata.org.
  12. [14] . wikidata.org.
  13. [15] . ddrare.nibiohn.go.jp. Retrieved . ddrare.nibiohn.go.jp. Provenance: wikidata.org.
  14. [16] . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  15. [17] . Disease Ontology. Retrieved . wikidata.org.
  16. [18] . wikidata.org.
  17. [19] . Phenocarta. Retrieved . gemma.msl.ubc.ca. Provenance: wikidata.org.
  18. [20] . Phenocarta. Retrieved . gemma.msl.ubc.ca. Provenance: wikidata.org.
  19. [21] . Phenocarta. Retrieved . gemma.msl.ubc.ca. Provenance: wikidata.org.
  20. [22] . Phenocarta. Retrieved . gemma.msl.ubc.ca. Provenance: wikidata.org.
  21. [23] . Phenocarta. Retrieved . gemma.msl.ubc.ca. Provenance: wikidata.org.
  22. [24] . Phenocarta. Retrieved . gemma.msl.ubc.ca. Provenance: wikidata.org.
  23. [25] . Phenocarta. Retrieved . gemma.msl.ubc.ca. Provenance: 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] . Wikimedia Foundation. dumps.wikimedia.org.
  2. [28] . Wikidata sitelinks. wikidata.org.
  3. [29] . 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). progressive supranuclear palsy. Retrieved May 3, 2026, from https://4ort.xyz/entity/progressive-supranuclear-palsy
MLA “progressive supranuclear palsy.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/progressive-supranuclear-palsy.
BibTeX @misc{4ortxyz_progressive-supranuclear-palsy_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{progressive supranuclear palsy}}, year = {2026}, url = {https://4ort.xyz/entity/progressive-supranuclear-palsy}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): progressive supranuclear palsy — https://4ort.xyz/entity/progressive-supranuclear-palsy (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. 7d ago · Nyuhn · 2026-07-10 view diff on Wikidata ↗
    P14541 3LCrOJ
    "/* wbeditentity-update:0| */ QuickStatements 3.0 [[:toollabs:qs-dev/batch/40849|batch #40849]]: ZGBK ID"
  2. 14d ago · JhealdBatch bot · 2026-07-03 view diff on Wikidata ↗
    Subclass of movement disorders, frontotemporal degeneration with dementia, genetic neurodegenerative disease with dementia +3
    Named after
    Health specialty neurology
    Genetic association STX6, EIF2AK3, MOBP +4
    + 6 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"
Live feed via Wikidata EventStreams. New edits appear within minutes of being made on Wikidata.