Home › Entities › rare_disease › hereditary spastic paraplegia 43

hereditary spastic paraplegia 43

hereditary spastic paraplegia that has material basis in mutation in the C19ORF12 gene on chromosome 19q12
MedicalCondition rare_disease Q32143030
Press Enter · cited answer in seconds

Summary

hereditary spastic paraplegia 43 is a rare disease[1]. It is known by 7 alternative names across languages and contexts.[2]

Key Facts

  • Instance of: class of disease[3]
  • Subclass of: hereditary spastic paraplegia[4], autosomal recessive complex spastic paraplegia[5], autosomal recessive disease[6]
  • Health specialty: neurology[7]
  • Genetic association: C19orf12[8]
  • Exact match: http://purl.obolibrary.org/obo/DOID_0110795[9], http://identifiers.org/doid/DOID:0110795[10], http://www.orpha.net/ORDO/Orphanet_320370[11]
  • On focus list of Wikimedia project: WikiProject Medicine[12]

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] ↑ . Disease Ontology. Retrieved . wikidata.org.
  5. [7] ↑ . wikidata.org.
  6. [8] ↑ . UniProt. Retrieved . wikidata.org.
  7. [9] ↑ . Disease Ontology. Retrieved . wikidata.org.
  8. [10] ↑ . Identifiers.org. registry.identifiers.org. Provenance: wikidata.org.
  9. [11] ↑ . wikidata.org.
  10. [12] ↑ . 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 43. Retrieved May 3, 2026, from https://4ort.xyz/entity/hereditary-spastic-paraplegia-43
MLA “hereditary spastic paraplegia 43.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/hereditary-spastic-paraplegia-43.
BibTeX @misc{4ortxyz_hereditary-spastic-paraplegia-43_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{hereditary spastic paraplegia 43}}, year = {2026}, url = {https://4ort.xyz/entity/hereditary-spastic-paraplegia-43}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): hereditary spastic paraplegia 43 — https://4ort.xyz/entity/hereditary-spastic-paraplegia-43 (retrieved 2026-05-03)

Canonical URL: https://4ort.xyz/entity/hereditary-spastic-paraplegia-43 · 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. 14w ago · JhealdBatch bot · 2026-07-05 view diff on Wikidata ↗
    Mondo id → MONDO_0014024
    Imported from → —
    Umls cui → C2680446
    Disease ontology id → DOID:0110795
    + 11 other properties edited (see Wikidata diff for full list)
    "/* wbeditentity-update:0| */ QuickStatements 3.0 [[:toollabs:qs-dev/batch/39953|batch #39953]]: deprecate redundant disease superclasses (2)"
Live feed via Wikidata EventStreams. New edits appear within minutes of being made on Wikidata.