X-linked progressive cerebellar ataxia

human disease
MedicalCondition developmental_defect_during_embryogenesis Q55345743
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Summary

X-linked progressive cerebellar ataxia is a developmental defect during embryogenesis[1]. It is known by 7 alternative names across languages and contexts.[2]

Key Facts

  • Instance of: rare disease[3], class of disease[4]
  • Subclass of: X-linked cerebellar ataxia[5], X-linked intellectual disability[6]
  • Genetic association: ATP2B3[7]
  • Exact match: http://www.orpha.net/ORDO/Orphanet_1175[8]

📑 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). X-linked progressive cerebellar ataxia. Retrieved May 3, 2026, from https://4ort.xyz/entity/x-linked-progressive-cerebellar-ataxia
MLA “X-linked progressive cerebellar ataxia.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/x-linked-progressive-cerebellar-ataxia.
BibTeX @misc{4ortxyz_x-linked-progressive-cerebellar-ataxia_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{X-linked progressive cerebellar ataxia}}, year = {2026}, url = {https://4ort.xyz/entity/x-linked-progressive-cerebellar-ataxia}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): X-linked progressive cerebellar ataxia — https://4ort.xyz/entity/x-linked-progressive-cerebellar-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. 15w ago · JhealdBatch bot · 2026-07-03 view diff on Wikidata ↗
    Mondo id → MONDO_0010547
    Genetic association → ATP2B3
    Orphanet id → 1175
    Instance of → developmental defect during embryogenesis, rare disease, class of disease
    + 9 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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