Roberts syndrome
type: Thing
description: Human disease
additional property: PropertyValue
  property ID: P31
  value: rare disease
additional property: PropertyValue
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  value: class of disease
additional property: PropertyValue
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additional property: PropertyValue
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  value: SC phocomelia syndrome
additional property: PropertyValue
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  value: syndrome
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  value: Roberts syndrome
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additional property: PropertyValue
  property ID: P2293
  value: ESCO2
additional property: PropertyValue
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additional property: PropertyValue
  property ID: P7464
  value: roberts-syndrome
confidence:
  popularity graph score:
    score: 0.01
    score pct: 1
    tier: long_tail
    components:
      sitelinks: 11
      sitelinks norm: 0.026
      unique citations: 4
      unique citations norm: 0.002
      monthly pageviews: 0
      monthly pageviews norm: 0.0
  sitelinks: 11
  unique citations: 4
  monthly pageviews: 0
  yearly pageviews: 378
  pageview trend:
    m: 2026-06
    v: 233
  pageview trend:
    m: 2026-05
    v: 71
  pageview trend:
    m: 2026-05
    v: 1
  pageview trend:
    m: 2026-05
    v: 3
  pageview trend:
    m: 2026-04
    v: 1
  pageview trend:
    m: 2026-04
    v: 4
  pageview trend:
    m: 2026-04
    v: 64
  pageview trend:
    m: 2026-04
    v: 1
  popularity:
    sitelinks: 11
    max: 423
    pct: 2.6
  tier: long_tail
claims:
  P31:
    value: Q929833
    source count: 0
    confidence: 0.0
    value label: rare disease
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    value: Q112193867
    source count: 0
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    value label: class of disease
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    value label: John Bingham Roberts
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    value label: syndrome
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    value: Roberts syndrome
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    value: 3103
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  P1995:
    value: Q1071953
    source count: 0
    confidence: 0.0
    value label: medical genetics

value: Q18052333
source count: 1
confidence: 0.2
value label: ESCO2

value: http://purl.obolibrary.org/obo/DOID_5325
source count: 1
confidence: 0.2

value: http://identifiers.org/doid/DOID:5325
source count: 1
confidence: 0.2

value: C0392475
source count: 1
confidence: 0.2

value: 7387
source count: 0
confidence: 0.0

value: Q4099686
source count: 0
confidence: 0.0
value label: WikiProject Medicine

value: 2777274139
source count: 0
confidence: 0.0

value: roberts-syndrome
source count: 0
confidence: 0.0

source: Identifiers.org
stated in qid: Q16335166

source: Freebase Data Dumps
stated in qid: Q15241312
pub year: 2013

source: Disease Ontology
stated in qid: Q5282129
retrieved: 2020-11-30

source: Roberts syndrome is caused by mutations in ESCO2, a human homolog of yeast ECO1 that is essential for the establishment of sister chromatid cohesion
stated in qid: Q34410361

wikidata id: Q619428
domain: rare_disease
level: standard
html url: https://4ort.xyz/entity/roberts-syndrome
markdown url: https://4ort.xyz/entity/roberts-syndrome.md
facts url summary: https://4ort.xyz/entity/roberts-syndrome/facts.json
facts url standard: https://4ort.xyz/entity/roberts-syndrome/facts.json
facts url full: https://4ort.xyz/entity/roberts-syndrome/facts.json
data source: Wikidata (CC0 / public domain)
license: https://creativecommons.org/publicdomain/zero/1.0/
api version: v1
served at: 2026-08-05T02:20:55.535899Z
entity updated at: 2026-05-03T21:19:00.258443+00:00Z
entity created at: 2026-04-10T23:48:51.774911+00:00Z