Joubert syndrome and related disorders

MedicalCondition developmental_defect_during_embryogenesis Q55345933
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Joubert syndrome and related disorders

Summary

Joubert syndrome and related disorders is a developmental defect during embryogenesis[1].

Key Facts

  • Joubert syndrome and related disorders's instance of is recorded as developmental defect during embryogenesis[2].
  • Joubert syndrome and related disorders's instance of is recorded as designated intractable/rare disease[3].
  • Joubert syndrome and related disorders's instance of is recorded as class of disease[4].
  • Joubert syndrome and related disorders is a type of autosomal recessive congenital cerebellar ataxia[5].
  • Joubert syndrome and related disorders's external data available at URL is recorded as http://www.nanbyou.or.jp/entry/4552[6].
  • Joubert syndrome and related disorders's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_140874[7].

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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). Joubert syndrome and related disorders. Retrieved May 3, 2026, from https://4ort.xyz/entity/joubert-syndrome-and-related-disorders
MLA “Joubert syndrome and related disorders.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/joubert-syndrome-and-related-disorders.
BibTeX @misc{4ortxyz_joubert-syndrome-and-related-disorders_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{Joubert syndrome and related disorders}}, year = {2026}, url = {https://4ort.xyz/entity/joubert-syndrome-and-related-disorders}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): Joubert syndrome and related disorders — https://4ort.xyz/entity/joubert-syndrome-and-related-disorders (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. 21h ago · JhealdBatch bot · 2026-07-03 view diff on Wikidata ↗
    Mondo id MONDO_0015369
    Orphanet id 140874
    Instance of developmental defect during embryogenesis, designated intractable/rare disease, class of disease
    Imported from
    + 4 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"
Live feed via Wikidata EventStreams. New edits appear within minutes of being made on Wikidata.