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Joubert syndrome 33

human disease
MedicalCondition developmental_defect_during_embryogenesis Q53661623
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Joubert syndrome 33

Summary

Joubert syndrome 33 is a developmental defect during embryogenesis[1]. It is known by 3 alternative names across languages and contexts.[2]

Key Facts

  • Joubert syndrome 33's instance of is recorded as developmental defect during embryogenesis[3].
  • Joubert syndrome 33's instance of is recorded as class of disease[4].
  • Joubert syndrome 33 is a type of Joubert syndrome[5].
  • Joubert syndrome 33's genetic association is recorded as PIBF1[6].
  • Joubert syndrome 33's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0080279[7].
  • Joubert syndrome 33's exact match is recorded as http://identifiers.org/doid/DOID:0080279[8].
  • Joubert syndrome 33's on focus list of Wikimedia project is recorded as WikiProject Medicine[9].

Why It Matters

Joubert syndrome 33 is known by 3 alternative names across languages and contexts.[2]

References

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

Direct Wikidata claims

  1. [3] ↑ . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  2. [4] ↑ . wikidata.org.
  3. [5] ↑ . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  4. [6] ↑ . Q905695. Retrieved . wikidata.org.
  5. [7] ↑ . Disease Ontology. Retrieved . wikidata.org.
  6. [8] ↑ . Identifiers.org. registry.identifiers.org. Provenance: wikidata.org.
  7. [9] ↑ . 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). Joubert syndrome 33. Retrieved May 3, 2026, from https://4ort.xyz/entity/joubert-syndrome-33
MLA “Joubert syndrome 33.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/joubert-syndrome-33.
BibTeX @misc{4ortxyz_joubert-syndrome-33_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{Joubert syndrome 33}}, year = {2026}, url = {https://4ort.xyz/entity/joubert-syndrome-33}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): Joubert syndrome 33 — https://4ort.xyz/entity/joubert-syndrome-33 (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. 11w ago · JhealdBatch bot · 2026-07-03 view diff on Wikidata ↗
    Mondo id → MONDO_0033311
    Genetic association → PIBF1
    Instance of → developmental defect during embryogenesis, class of disease
    Imported from → —
    + 8 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.