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spinocerebellar ataxia type 42

human disease
MedicalCondition rare_disease Q55345906
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Summary

spinocerebellar ataxia type 42 is a rare disease[1]. It is known by 4 alternative names across languages and contexts.[2]

Key Facts

  • Instance of: class of disease[3]
  • Subclass of: autosomal dominant cerebellar ataxia type III[4], spinocerebellar ataxia[5], developmental defect during embryogenesis[6]
  • Prevalence: 0.000001[7]
  • NCI Thesaurus ID: C171269[8]
  • Genetic association: CACNA1G[9]
  • Age of onset: juvenile onset[10], adult onset[11], childhood onset[12], late onset[13]
  • Exact match: http://www.orpha.net/ORDO/Orphanet_458803[14], http://purl.obolibrary.org/obo/DOID_0111742[15], http://identifiers.org/doid/DOID:0111742[16]
  • Has phenotype: diplopia[17], erectile dysfunction[18], scoliosis[19], psoriasis[20], Q141816420[21]
  • P14914: D458803[22]

References

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

Direct Wikidata claims

  1. [3] ↑ . wikidata.org.
  2. [4] ↑ . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  3. [5] ↑ . Disease Ontology. Retrieved . wikidata.org.
  4. [6] ↑ . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  5. [7] ↑ . Retrieved . wikidata.org.
  6. [8] ↑ . wikidata.org.
  7. [9] ↑ . UniProt. Retrieved . platform.opentargets.org. Provenance: wikidata.org.
  8. [10] ↑ . Retrieved . wikidata.org.
  9. [11] ↑ . Retrieved . wikidata.org.
  10. [12] ↑ . Retrieved . wikidata.org.
  11. [13] ↑ . Retrieved . wikidata.org.
  12. [14] ↑ . wikidata.org.
  13. [15] ↑ . Disease Ontology. Retrieved . wikidata.org.
  14. [16] ↑ . Identifiers.org. registry.identifiers.org. Provenance: wikidata.org.
  15. [17] ↑ . Retrieved . wikidata.org.
  16. [18] ↑ . Retrieved . wikidata.org.
  17. [19] ↑ . Retrieved . wikidata.org.
  18. [20] ↑ . Retrieved . wikidata.org.
  19. [21] ↑ . Retrieved . 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). spinocerebellar ataxia type 42. Retrieved October 24, 2026, from https://4ort.xyz/entity/spinocerebellar-ataxia-type-42
MLA “spinocerebellar ataxia type 42.” 4ort.xyz Knowledge Graph, 4ort.xyz, 24 Oct. 2026, https://4ort.xyz/entity/spinocerebellar-ataxia-type-42.
BibTeX @misc{4ortxyz_spinocerebellar-ataxia-type-42_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{spinocerebellar ataxia type 42}}, year = {2026}, url = {https://4ort.xyz/entity/spinocerebellar-ataxia-type-42}, note = {Accessed: 2026-10-24}}
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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. 9h ago · ACorrêa (WMB) · 2026-10-24 view diff on Wikidata ↗
    Prevalence → {'amount': '+0.000001'}
    Age of onset → juvenile onset, adult onset, childhood onset +1
    Has phenotype → diplopia, erectile dysfunction, scoliosis +2
    P14914 → D458803
    + 1 other property edited (see Wikidata diff for full list)
    "/* 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 · 2026-07-03 view diff on Wikidata ↗
    Mondo id → MONDO_0014776
    Genetic association → CACNA1G
    Orphanet id → 458803
    Instance of → rare disease, class of disease
    + 11 other properties edited (see Wikidata diff for full list)
    "/* wbeditentity-update:0| */ QuickStatements 3.0 [[:toollabs:qs-dev/batch/39742|batch #39742]]: subclass of disease, not instance"
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