Gordon syndrome
type: Thing
description: medical condition
additional property: PropertyValue
  property ID: P31
  value: rare disease
additional property: PropertyValue
  property ID: P31
  value: class of disease
additional property: PropertyValue
  property ID: P279
  value: distal arthrogryposis type 3
additional property: PropertyValue
  property ID: P486
  value: C537288
additional property: PropertyValue
  property ID: P492
  value: 114300
additional property: PropertyValue
  property ID: P646
  value: /m/010943v9
additional property: PropertyValue
  property ID: P1550
  value: 376
additional property: PropertyValue
  property ID: P2293
  value: PIEZO2
additional property: PropertyValue
  property ID: P2892
  value: C0220666
additional property: PropertyValue
  property ID: P4317
  value: 2553
additional property: PropertyValue
  property ID: P6366
  value: 2779619945
additional property: PropertyValue
  property ID: P10565
  value: 170906
confidence:
  popularity graph score:
    score: 0.0
    score pct: 0
    tier: long_tail
    components:
      sitelinks: 0
      sitelinks norm: 0.0
      unique citations: 2
      unique citations norm: 0.001
      monthly pageviews: 131
      monthly pageviews norm: 0.0
  sitelinks: 0
  unique citations: 2
  monthly pageviews: 131
  yearly pageviews: 144
  pageview trend:
    m: 2026-07
    v: 131
  pageview trend:
    m: 2026-06
    v: 10
  pageview trend:
    m: 2026-05
    v: 3
  tier: long_tail
claims:
  P31:
    value: Q929833
    source count: 0
    confidence: 0.0
    value label: rare disease
  P31:
    value: Q112193867
    source count: 0
    confidence: 0.0
    value label: class of disease
  P279:
    value: Q102293313
    source count: 0
    confidence: 0.0
    value label: distal arthrogryposis type 3
  P486:
    value: C537288
    source count: 0
    confidence: 0.0
  P492:
    value: 114300
    source count: 0
    confidence: 0.0
  P646:
    value: /m/010943v9
    source count: 0
    confidence: 0.0
  P1550:
    value: 376
    source count: 0
    confidence: 0.0
  P2293:
    value: Q18045483
    source count: 1
    confidence: 0.2
    value label: PIEZO2
  P2892:
    value: C0220666
    source count: 1
    confidence: 0.2
  P4317:
    value: 2553
    source count: 0
    confidence: 0.0
  P6366:
    value: 2779619945
    source count: 0
    confidence: 0.0
  P10565:
    value: 170906
    source count: 0
    confidence: 0.0
citations:
  source: UMLS 2023
  stated in qid: Q118645236
  retrieved: 2023-05-25
citations:
  source: Mutations in PIEZO2 cause Gordon syndrome, Marden-Walker syndrome, and distal arthrogryposis type 5.
  stated in qid: Q30426893
meta:
  wikidata id: Q16866974
  domain: rare_disease
  level: standard
  html url: https://4ort.xyz/entity/gordon-syndrome
  markdown url: https://4ort.xyz/entity/gordon-syndrome.md
  facts url summary: https://4ort.xyz/entity/gordon-syndrome/facts.json
  facts url standard: https://4ort.xyz/entity/gordon-syndrome/facts.json
  facts url full: https://4ort.xyz/entity/gordon-syndrome/facts.json
  data source: Wikidata (CC0 / public domain)
  license: https://creativecommons.org/publicdomain/zero/1.0/
  api version: v1
  served at: 2026-08-08T12:51:14.182270Z
  entity updated at: 2026-05-03T21:19:00.258443+00:00Z
  entity created at: 2026-05-03T14:11:27.902680+00:00Z