Crouzon syndrome

Congenital disorder of the skull and face
MedicalCondition developmental_defect_during_embryogenesis Q779250
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Crouzon syndrome

Summary

Crouzon syndrome is a developmental defect during embryogenesis[1]. It ranks in the top 6% of developmental_defect_during_embryogenesis entities by monthly Wikipedia readership (1,433 views/month).[2]

Key Facts

  • Crouzon syndrome's instance of is recorded as developmental defect during embryogenesis[3].
  • Crouzon syndrome's instance of is recorded as designated intractable/rare disease[4].
  • Crouzon syndrome's instance of is recorded as rare disease[5].
  • Crouzon syndrome's instance of is recorded as class of disease[6].
  • Crouzon syndrome's instance of is recorded as symptom or sign[7].
  • Octave Crouzon is named after Crouzon syndrome[8].
  • Crouzon syndrome is a type of craniosynostosis[9].
  • Crouzon syndrome is a type of craniostenosis associated with a strabismus[10].
  • Crouzon syndrome is a type of syndromic craniosynostosis[11].
  • Crouzon syndrome is a type of disease[12].
  • Crouzon syndrome's Commons category is recorded as Crouzon syndrome[13].
  • Crouzon syndrome's ICPC 2 ID is recorded as L82[14].
  • Crouzon syndrome's external data available at URL is recorded as http://www.nanbyou.or.jp/entry/4672[15].
  • Crouzon syndrome's NCI Thesaurus ID is recorded as C84653[16].
  • Crouzon syndrome's health specialty is recorded as medical genetics[17].
  • Crouzon syndrome's genetic association is recorded as FGFR2[18].
  • Crouzon syndrome's exact match is recorded as http://purl.obolibrary.org/obo/DOID_2339[19].
  • Crouzon syndrome's exact match is recorded as http://identifiers.org/doid/DOID:2339[20].
  • Crouzon syndrome's exact match is recorded as http://purl.obolibrary.org/obo/HP_0004439[21].
  • Crouzon syndrome's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_207[22].
  • Crouzon syndrome's on focus list of Wikimedia project is recorded as WikiProject Medicine[23].

Why It Matters

Crouzon syndrome ranks in the top 6% of developmental_defect_during_embryogenesis entities by monthly Wikipedia readership (1,433 views/month).[2] It has Wikipedia articles in 15 language editions, a strong signal of global cultural recognition.[24] It is known by 13 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] . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  2. [4] . ddrare.nibiohn.go.jp. Retrieved . ddrare.nibiohn.go.jp. Provenance: wikidata.org.
  3. [5] . wikidata.org.
  4. [6] . wikidata.org.
  5. [7] . wikidata.org.
  6. [8] . wikidata.org.
  7. [9] . Disease Ontology. Retrieved . wikidata.org.
  8. [10] . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  9. [11] . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  10. [12] . wikidata.org.
  11. [13] . wikidata.org.
  12. [14] . wikidata.org.
  13. [15] . ddrare.nibiohn.go.jp. Retrieved . ddrare.nibiohn.go.jp. Provenance: wikidata.org.
  14. [16] . Disease Ontology. Retrieved . wikidata.org.
  15. [17] . wikidata.org.
  16. [18] . Q905695. Retrieved . search.clinicalgenome.org. Provenance: wikidata.org.
  17. [19] . Disease Ontology. Retrieved . wikidata.org.
  18. [20] . Identifiers.org. registry.identifiers.org. Provenance: wikidata.org.
  19. [21] . Human Phenotype Ontology release 2018-03-08. Retrieved . wikidata.org.
  20. [22] . wikidata.org.
  21. [23] . wikidata.org.

Class ancestry

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

Aggregate / graph-position facts

  1. [2] . Wikimedia Foundation. dumps.wikimedia.org.
  2. [24] . Wikidata sitelinks. wikidata.org.
  3. [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). Crouzon syndrome. Retrieved May 3, 2026, from https://4ort.xyz/entity/crouzon-syndrome
MLA “Crouzon syndrome.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/crouzon-syndrome.
BibTeX @misc{4ortxyz_crouzon-syndrome_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{Crouzon syndrome}}, year = {2026}, url = {https://4ort.xyz/entity/crouzon-syndrome}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): Crouzon syndrome — https://4ort.xyz/entity/crouzon-syndrome (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. 12d ago · Twofivesixbot bot · 2026-05-20 view diff on Wikidata ↗
    On focus list of wikimedia project WikiProject Medicine
    Named after Octave Crouzon
    Instance of
    Subclass of craniosynostosis, craniostenosis associated with a strabismus, syndromic craniosynostosis +1
    + 6 other properties edited (see Wikidata diff for full list)
    "/* wbsetclaim-update-qualifiers:1||1|11 */ [[Property:P2347]]: 39534, mv to monolingual text names on YSO statements"
Live feed via Wikidata EventStreams. New edits appear within minutes of being made on Wikidata.