spinocerebellar ataxia

group of dominantly inherited, predominately late-onset, cerebellar ataxias. Neuro-developmental outcome and brain-derived neurotrophic factor level in relation to feeding practice in early infancy.
MedicalCondition designated_intractable_rare_disease Q899726
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spinocerebellar ataxia

Summary

spinocerebellar ataxia is a designated intractable/rare disease[1]. It has Wikipedia articles in 20 language editions, a strong signal of global cultural recognition.[2]

Key Facts

  • spinocerebellar ataxia's instance of is recorded as designated intractable/rare disease[3].
  • spinocerebellar ataxia's instance of is recorded as class of disease[4].
  • spinocerebellar ataxia's instance of is recorded as symptom or sign[5].
  • spinocerebellar ataxia is a type of hereditary ataxia[6].
  • spinocerebellar ataxia is a type of late-onset ataxia with dementia[7].
  • spinocerebellar ataxia is a type of nervous system heredodegenerative disease[8].
  • spinocerebellar ataxia is a type of eye degenerative disease[9].
  • spinocerebellar ataxia is a type of cerebral degeneration[10].
  • spinocerebellar ataxia is a type of autosomal dominant disease[11].
  • spinocerebellar ataxia is a type of spinocerebellar degenerations[12].
  • spinocerebellar ataxia is a type of cerebellar ataxia[13].
  • spinocerebellar ataxia is a type of disease[14].
  • spinocerebellar ataxia's ICPC 2 ID is recorded as N99[15].
  • spinocerebellar ataxia's external data available at URL is recorded as http://www.nanbyou.or.jp/entry/4879[16].
  • spinocerebellar ataxia's ICD-9-CM is recorded as 334.3[17].
  • spinocerebellar ataxia's NCI Thesaurus ID is recorded as C82341[18].
  • spinocerebellar ataxia's health specialty is recorded as neurology[19].
  • spinocerebellar ataxia's exact match is recorded as http://purl.obolibrary.org/obo/DOID_1441[20].
  • spinocerebellar ataxia's exact match is recorded as http://identifiers.org/doid/DOID:1441[21].
  • spinocerebellar ataxia's exact match is recorded as http://purl.obolibrary.org/obo/HP_0007263[22].
  • spinocerebellar ataxia's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_99[23].
  • spinocerebellar ataxia's on focus list of Wikimedia project is recorded as WikiProject Medicine[24].

Why It Matters

spinocerebellar ataxia has Wikipedia articles in 20 language editions, a strong signal of global cultural recognition.[2] It is known by 38 alternative names across languages and contexts.[25]

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] . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  6. [8] . Monarch Disease Ontology release 2018-06-29. 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] . Disease Ontology. Retrieved . wikidata.org.
  10. [12] . wikidata.org.
  11. [13] . Disease Ontology. Retrieved . wikidata.org.
  12. [14] . wikidata.org.
  13. [15] . wikidata.org.
  14. [16] . ddrare.nibiohn.go.jp. Retrieved . ddrare.nibiohn.go.jp. Provenance: wikidata.org.
  15. [17] . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  16. [18] . Disease Ontology. Retrieved . wikidata.org.
  17. [19] . wikidata.org.
  18. [20] . Disease Ontology. Retrieved . wikidata.org.
  19. [21] . Identifiers.org. registry.identifiers.org. Provenance: wikidata.org.
  20. [22] . Human Phenotype Ontology release 2018-03-08. Retrieved . wikidata.org.
  21. [23] . wikidata.org.
  22. [24] . wikidata.org.

Class ancestry

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

Aggregate / graph-position facts

  1. [2] . Wikidata sitelinks. wikidata.org.
  2. [25] . 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. Retrieved May 3, 2026, from https://4ort.xyz/entity/spinocerebellar-ataxia
MLA “spinocerebellar ataxia.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/spinocerebellar-ataxia.
BibTeX @misc{4ortxyz_spinocerebellar-ataxia_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{spinocerebellar ataxia}}, year = {2026}, url = {https://4ort.xyz/entity/spinocerebellar-ataxia}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): spinocerebellar ataxia — https://4ort.xyz/entity/spinocerebellar-ataxia (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. 16h ago · JhealdBatch bot · 2026-07-03 view diff on Wikidata ↗
    Subclass of hereditary ataxia, late-onset ataxia with dementia, nervous system heredodegenerative disease +6
    Health specialty neurology
    Subclass of
    Instance of designated intractable/rare disease, class of disease, symptom or sign
    + 3 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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