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craniosynostosis

premature fusion of bones in the skull
MedicalCondition class_of_disease Q378183
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craniosynostosis

Summary

craniosynostosis is a class of disease[1]. craniosynostosis draws 1,040 Wikipedia views per month (class_of_disease category, ranking #374 of 1,968).[2]

Key Facts

  • craniosynostosis's instance of is recorded as class of disease[3].
  • craniosynostosis is a type of synostosis[4].
  • craniosynostosis is a type of rare disease[5].
  • craniosynostosis is a type of craniofacial disease[6].
  • craniosynostosis is a type of disease[7].
  • craniosynostosis's Commons category is recorded as Craniosynostosis[8].
  • craniosynostosis's ICPC 2 ID is recorded as L82[9].
  • craniosynostosis's prevalence is recorded as {'amount': '+0.000045'}[10].
  • craniosynostosis's NCI Thesaurus ID is recorded as C84655[11].
  • craniosynostosis's health specialty is recorded as medical genetics[12].
  • craniosynostosis's genetic association is recorded as BBS9[13].
  • craniosynostosis's genetic association is recorded as TWIST1[14].
  • craniosynostosis's genetic association is recorded as TCF12[15].
  • craniosynostosis's genetic association is recorded as SKI[16].
  • craniosynostosis's genetic association is recorded as ERF[17].
  • craniosynostosis's genetic association is recorded as MSX2[18].
  • craniosynostosis's genetic association is recorded as FGFR2[19].
  • craniosynostosis's exact match is recorded as http://purl.obolibrary.org/obo/DOID_2340[20].
  • craniosynostosis's exact match is recorded as http://identifiers.org/doid/DOID:2340[21].
  • craniosynostosis's exact match is recorded as http://purl.obolibrary.org/obo/HP_0000243[22].
  • craniosynostosis's exact match is recorded as http://purl.obolibrary.org/obo/HP_0000262[23].
  • craniosynostosis's exact match is recorded as http://purl.obolibrary.org/obo/HP_0000263[24].
  • craniosynostosis's exact match is recorded as http://purl.obolibrary.org/obo/HP_0001363[25].
  • craniosynostosis's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_1531[26].
  • craniosynostosis's on focus list of Wikimedia project is recorded as WikiProject Medicine[27].

Why It Matters

craniosynostosis draws 1,040 Wikipedia views per month (class_of_disease category, ranking #374 of 1,968).[2] craniosynostosis has Wikipedia articles in 18 language editions, a strong signal of global cultural recognition.[28] craniosynostosis is known by 6 alternative names across languages and contexts.[29]

Related Entities

disease

References

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

Direct Wikidata claims

  1. [3] ↑ . wikidata.org.
  2. [4] ↑ . Disease Ontology. Retrieved . wikidata.org.
  3. [5] ↑ . Q1515833. orpha.net. Provenance: wikidata.org.
  4. [6] ↑ . wikidata.org.
  5. [7] ↑ . wikidata.org.
  6. [8] ↑ . wikidata.org.
  7. [9] ↑ . wikidata.org.
  8. [10] ↑ . Q1515833. Retrieved . orpha.net. Provenance: wikidata.org.
  9. [11] ↑ . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  10. [12] ↑ . wikidata.org.
  11. [13] ↑ . Phenocarta. Retrieved . gemma.msl.ubc.ca. Provenance: wikidata.org.
  12. [14] ↑ . Isolated sagittal and coronal craniosynostosis associated with TWIST box mutations. wikidata.org.
  13. [15] ↑ . Mutations in TCF12, encoding a basic helix-loop-helix partner of TWIST1, are a frequent cause of coronal craniosynostosis. wikidata.org.
  14. [16] ↑ . Mutations in the TGF-β repressor SKI cause Shprintzen-Goldberg syndrome with aortic aneurysm. wikidata.org.
  15. [17] ↑ . Reduced dosage of ERF causes complex craniosynostosis in humans and mice and links ERK1/2 signaling to regulation of osteogenesis. wikidata.org.
  16. [18] ↑ . A mutation in the homeodomain of the human MSX2 gene in a family affected with autosomal dominant craniosynostosis. wikidata.org.
  17. [19] ↑ . Open Targets Platform. Retrieved . platform.opentargets.org. Provenance: 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] ↑ . Human Phenotype Ontology release 2018-03-08. Retrieved . wikidata.org.
  22. [24] ↑ . Human Phenotype Ontology release 2018-03-08. Retrieved . wikidata.org.
  23. [25] ↑ . Human Phenotype Ontology release 2018-03-08. Retrieved . wikidata.org.
  24. [26] ↑ . wikidata.org.
  25. [27] ↑ . wikidata.org.

Class ancestry

  1. [1] ↑ . Wikidata. wikidata.org.

Aggregate / graph-position facts

  1. [2] ↑ . Wikimedia Foundation. dumps.wikimedia.org.
  2. [28] ↑ . Wikidata sitelinks. wikidata.org.
  3. [29] ↑ . 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). craniosynostosis. Retrieved May 3, 2026, from https://4ort.xyz/entity/craniosynostosis
MLA “craniosynostosis.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/craniosynostosis.
BibTeX @misc{4ortxyz_craniosynostosis_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{craniosynostosis}}, year = {2026}, url = {https://4ort.xyz/entity/craniosynostosis}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): craniosynostosis — https://4ort.xyz/entity/craniosynostosis (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. 4d ago · Twofivesixbot bot · 2026-05-19 view diff on Wikidata ↗
    Prevalence → {'amount': '+0.000045'}
    Subclass of → synostosis, rare disease, craniofacial disease +1
    Instance of → —
    Aliases → —
    + 5 other properties edited (see Wikidata diff for full list)
    "/* wbsetclaim-update-qualifiers:1||1|9 */ [[Property:P2347]]: 28456, mv to monolingual text names on YSO statements"
Live feed via Wikidata EventStreams. New edits appear within minutes of being made on Wikidata.