Greig cephalopolysyndactyly syndrome

acrocephalosyndactylia that has material basis in mutation in the GLI3 gene which results in abnormal development located in limb, located in head, located in face
MedicalCondition developmental_defect_during_embryogenesis Q3508649
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Greig cephalopolysyndactyly syndrome

Summary

Greig cephalopolysyndactyly syndrome is a developmental defect during embryogenesis[1]. It has Wikipedia articles in 7 language editions, a strong signal of global cultural recognition.[2]

Key Facts

  • Greig cephalopolysyndactyly syndrome's instance of is recorded as developmental defect during embryogenesis[3].
  • Greig cephalopolysyndactyly syndrome's instance of is recorded as rare disease[4].
  • Greig cephalopolysyndactyly syndrome's instance of is recorded as class of disease[5].
  • David Middleton Greig is named after Greig cephalopolysyndactyly syndrome[6].
  • Greig cephalopolysyndactyly syndrome is a type of acrocephalosyndactylia[7].
  • Greig cephalopolysyndactyly syndrome is a type of syndrome with limb duplication, polydactyly, syndactyly, and/or hyperphalangy[8].
  • Greig cephalopolysyndactyly syndrome is a type of genetic disease[9].
  • Greig cephalopolysyndactyly syndrome is a type of autosomal dominant disease[10].
  • Greig cephalopolysyndactyly syndrome's Commons category is recorded as Greig syndrome[11].
  • Greig cephalopolysyndactyly syndrome's NCI Thesaurus ID is recorded as C35255[12].
  • Greig cephalopolysyndactyly syndrome's genetic association is recorded as GLI3[13].
  • Greig cephalopolysyndactyly syndrome's exact match is recorded as http://purl.obolibrary.org/obo/DOID_14761[14].
  • Greig cephalopolysyndactyly syndrome's exact match is recorded as http://identifiers.org/doid/DOID:14761[15].
  • Greig cephalopolysyndactyly syndrome's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_380[16].
  • Greig cephalopolysyndactyly syndrome's on focus list of Wikimedia project is recorded as WikiProject Medicine[17].

Why It Matters

Greig cephalopolysyndactyly syndrome has Wikipedia articles in 7 language editions, a strong signal of global cultural recognition.[2] It is known by 10 alternative names across languages and contexts.[18]

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] . wikidata.org.
  4. [6] . wikidata.org.
  5. [7] . Disease Ontology. Retrieved . wikidata.org.
  6. [8] . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  7. [9] . Disease Ontology. Retrieved . wikidata.org.
  8. [10] . Disease Ontology. Retrieved . wikidata.org.
  9. [11] . wikidata.org.
  10. [12] . Disease Ontology. Retrieved . wikidata.org.
  11. [13] . Q905695. Retrieved . platform.opentargets.org. Provenance: wikidata.org.
  12. [14] . Disease Ontology. Retrieved . wikidata.org.
  13. [15] . Identifiers.org. registry.identifiers.org. Provenance: wikidata.org.
  14. [16] . wikidata.org.
  15. [17] . wikidata.org.

Class ancestry

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

Aggregate / graph-position facts

  1. [2] . Wikidata sitelinks. wikidata.org.
  2. [18] . 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). Greig cephalopolysyndactyly syndrome. Retrieved May 3, 2026, from https://4ort.xyz/entity/greig-cephalopolysyndactyly-syndrome
MLA “Greig cephalopolysyndactyly syndrome.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/greig-cephalopolysyndactyly-syndrome.
BibTeX @misc{4ortxyz_greig-cephalopolysyndactyly-syndrome_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{Greig cephalopolysyndactyly syndrome}}, year = {2026}, url = {https://4ort.xyz/entity/greig-cephalopolysyndactyly-syndrome}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): Greig cephalopolysyndactyly syndrome — https://4ort.xyz/entity/greig-cephalopolysyndactyly-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. 2d ago · JhealdBatch bot · 2026-07-03 view diff on Wikidata ↗
    Named after
    Genetic association GLI3
    Subclass of
    Instance of developmental defect during embryogenesis, rare disease, class of disease
    + 5 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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