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Gordon syndrome

medical condition
Class type of: distal arthrogryposis type 3 Q16866974

Facts

7 properties
Instance of
rare disease, class of disease[3]
Subclass of
distal arthrogryposis type 3
Age of onset
congenital onset, neonatal onset[5][6]
Genetic association
PIEZO2[4]
Has phenotype
talipes, Camptodactyly of finger, High-arched palate, cryptorchidism, cleft palate, facial asymmetry, deafness, pectus excavatum, Finger syndactyly[7][8][9][10][11][12][13][14][15]
P14541
hwHQS[16]
P14914
D00376[17]
🏷️ Also known as
en distal arthrogryposis type 3 en Gordon syndrome fr syndrome de Gordon
🔖 Identifiers · 8
Encyclopedia of China (Third Edition) ID
170906
Freebase ID
/m/010943v9
GARD rare disease ID
2553
MeSH descriptor ID
C537288
Microsoft Academic ID (discontinued)
2779619945
OMIM ID
114300
Orphanet ID
376
UMLS CUI
C0220666

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Summary

Gordon syndrome is a rare disease[1]. It is a type of distal arthrogryposis type 3[2].

References

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

Direct Wikidata claims

  1. [3] ↑ . wikidata.org.
  2. [2] ↑ . wikidata.org.
  3. [4] ↑ . Mutations in PIEZO2 cause Gordon syndrome, Marden-Walker syndrome, and distal arthrogryposis type 5.. wikidata.org.
  4. [5] ↑ . Retrieved . wikidata.org.
  5. [6] ↑ . Retrieved . wikidata.org.
  6. [7] ↑ . Retrieved . wikidata.org.
  7. [8] ↑ . Retrieved . wikidata.org.
  8. [9] ↑ . Retrieved . wikidata.org.
  9. [10] ↑ . Retrieved . wikidata.org.
  10. [11] ↑ . Retrieved . wikidata.org.
  11. [12] ↑ . Retrieved . wikidata.org.
  12. [13] ↑ . Retrieved . wikidata.org.
  13. [14] ↑ . Retrieved . wikidata.org.
  14. [15] ↑ . Retrieved . wikidata.org.
  15. [16] ↑ . wikidata.org.
  16. [17] ↑ . wikidata.org.

Class ancestry

  1. [1] ↑ . Wikidata. wikidata.org.

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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). Gordon syndrome. Retrieved November 3, 2026, from https://4ort.xyz/entity/gordon-syndrome
MLA “Gordon syndrome.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 Nov. 2026, https://4ort.xyz/entity/gordon-syndrome.
BibTeX @misc{4ortxyz_gordon-syndrome_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{Gordon syndrome}}, year = {2026}, url = {https://4ort.xyz/entity/gordon-syndrome}, note = {Accessed: 2026-11-03}}
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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. 10d ago · ACorrêa (WMB) · 2026-10-24 view diff on Wikidata ↗
    Sitelink count → 1
    Wikipedia languages → ['en']
    Age of onset → congenital onset, neonatal onset
    Has phenotype → talipes, Camptodactyly of finger, High-arched palate +6
    + 2 other properties edited (see Wikidata diff for full list)
    "/* wbeditentity-update-languages-and-other-short:0||pt, pt-br */ QuickStatements 3.0 [[:toollabs:qs-dev/batch/61469|batch #61469]]: Raras.org data import"
  2. 16w ago · Nyuhn · 2026-07-10 view diff on Wikidata ↗
    Imported from → —
    MeSH descriptor ID → C537288
    OMIM ID → 114300
    P14541 → hwHQS
    + 10 other properties edited (see Wikidata diff for full list)
    "/* wbeditentity-update:0| */ QuickStatements 3.0 [[:toollabs:qs-dev/batch/40849|batch #40849]]: ZGBK ID"
Live feed via Wikidata EventStreams. New edits appear within minutes of being made on Wikidata.