Home › Entities › rare_disease › hereditary spastic paraplegia 11

hereditary spastic paraplegia 11

hereditary spastic paraplegia that has material basis in mutation in the SPG11 gene on chromosome 15q21
MedicalCondition rare_disease Q32142563
Press Enter · cited answer in seconds

Summary

hereditary spastic paraplegia 11 is a rare disease[1]. It is known by 14 alternative names across languages and contexts.[2]

Key Facts

  • Instance of: class of disease[3]
  • Subclass of: hereditary spastic paraplegia[4], pure or complex autosomal recessive spastic paraplegia[5], complex hereditary spastic paraplegia[6], genetic syndromic intellectual disability[7], genetic disease[8], autosomal recessive disease[9]
  • Prevalence: 0.000005[10]
  • NCI Thesaurus ID: C148317[11]
  • Health specialty: neurology[12]
  • Genetic association: SPG11[13]
  • Age of onset: juvenile onset[14], adult onset[15], childhood onset[16], infantile onset[17]
  • Exact match: http://purl.obolibrary.org/obo/DOID_0110764[18], http://identifiers.org/doid/DOID:0110764[19], http://www.orpha.net/ORDO/Orphanet_2822[20]
  • On focus list of Wikimedia project: WikiProject Medicine[21]
  • P14914: D02822[22]

References

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

Direct Wikidata claims

  1. [3] ↑ . wikidata.org.
  2. [4] ↑ . Disease Ontology. Retrieved . wikidata.org.
  3. [5] ↑ . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  4. [6] ↑ . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  5. [7] ↑ . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  6. [8] ↑ . Disease Ontology. Retrieved . wikidata.org.
  7. [9] ↑ . Disease Ontology. Retrieved . wikidata.org.
  8. [10] ↑ . Retrieved . wikidata.org.
  9. [11] ↑ . wikidata.org.
  10. [12] ↑ . wikidata.org.
  11. [13] ↑ . UniProt. Retrieved . platform.opentargets.org. Provenance: wikidata.org.
  12. [14] ↑ . Retrieved . wikidata.org.
  13. [15] ↑ . Retrieved . wikidata.org.
  14. [16] ↑ . Retrieved . wikidata.org.
  15. [17] ↑ . Retrieved . wikidata.org.
  16. [18] ↑ . Disease Ontology. Retrieved . wikidata.org.
  17. [19] ↑ . Identifiers.org. registry.identifiers.org. Provenance: wikidata.org.
  18. [20] ↑ . wikidata.org.
  19. [21] ↑ . wikidata.org.
  20. [22] ↑ . wikidata.org.

Class ancestry

  1. [1] ↑ . Wikidata. wikidata.org.

Aggregate / graph-position facts

  1. [2] ↑ . 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). hereditary spastic paraplegia 11. Retrieved October 23, 2026, from https://4ort.xyz/entity/hereditary-spastic-paraplegia-11
MLA “hereditary spastic paraplegia 11.” 4ort.xyz Knowledge Graph, 4ort.xyz, 23 Oct. 2026, https://4ort.xyz/entity/hereditary-spastic-paraplegia-11.
BibTeX @misc{4ortxyz_hereditary-spastic-paraplegia-11_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{hereditary spastic paraplegia 11}}, year = {2026}, url = {https://4ort.xyz/entity/hereditary-spastic-paraplegia-11}, note = {Accessed: 2026-10-23}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): hereditary spastic paraplegia 11 — https://4ort.xyz/entity/hereditary-spastic-paraplegia-11 (retrieved 2026-10-23)

Canonical URL: https://4ort.xyz/entity/hereditary-spastic-paraplegia-11 · Last refreshed:

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 · ACorrêa (WMB) · 2026-10-23 view diff on Wikidata ↗
    Prevalence → {'amount': '+0.000005'}
    Age of onset → juvenile onset, adult onset, childhood onset +1
    P14914 → D02822
    Claims rich → —
    "/* wbeditentity-update-languages-and-other-short:0||pt, pt-br */ QuickStatements 3.0 [[:toollabs:qs-dev/batch/61469|batch #61469]]: Raras.org data import"
  2. 16w ago · JhealdBatch bot · 2026-07-05 view diff on Wikidata ↗
    Nci thesaurus id → C148317
    On focus list of wikimedia project → WikiProject Medicine
    Gard rare disease id → 4919
    Health specialty → neurology
    + 14 other properties edited (see Wikidata diff for full list)
    "/* wbeditentity-update:0| */ QuickStatements 3.0 [[:toollabs:qs-dev/batch/39943|batch #39943]]: deprecate redundant disease superclasses"
Live feed via Wikidata EventStreams. New edits appear within minutes of being made on Wikidata.