autosomal dominant mental retardation 55
type: Thing
description: human disease
additional property: PropertyValue
  property ID: P31
  value: class of disease
additional property: PropertyValue
  property ID: P279
  value: autosomal dominant disease
additional property: PropertyValue
  property ID: P279
  value: syndromic intellectual disability
additional property: PropertyValue
  property ID: P492
  value: 617831
additional property: PropertyValue
  property ID: P699
  value: DOID:0080227
additional property: PropertyValue
  property ID: P1550
  value: 442835
additional property: PropertyValue
  property ID: P2293
  value: NUS1
additional property: PropertyValue
  property ID: P2888
  value: http://purl.obolibrary.org/obo/DOID_0080227
additional property: PropertyValue
  property ID: P2888
  value: http://www.orpha.net/ORDO/Orphanet_442835
additional property: PropertyValue
  property ID: P5008
  value: WikiProject Medicine
additional property: PropertyValue
  property ID: P5270
  value: MONDO_0030921
additional property: PropertyValue
  property ID: P11430
  value: DI-05178
confidence:
  popularity graph score:
    score: 0.0
    score pct: 0
    tier: long_tail
    components:
      sitelinks: 0
      sitelinks norm: 0.0
      unique citations: 3
      unique citations norm: 0.001
      monthly pageviews: 0
      monthly pageviews norm: 0.0
  sitelinks: 0
  unique citations: 3
  monthly pageviews: 0
  yearly pageviews: 0
  tier: long_tail
claims:
  P31:
    value: Q112193867
    source count: 0
    confidence: 0.0
    value label: class of disease
  P279:
    value: Q18553439
    source count: 1
    confidence: 0.2
    value label: autosomal dominant disease
  P279:
    value: Q18553536
    source count: 1
    confidence: 0.2
    value label: syndromic intellectual disability
  P492:
    value: 617831
    source count: 2
    confidence: 0.4
  P699:
    value: DOID:0080227
    source count: 1
    confidence: 0.2
  P1550:
    value: 442835
    source count: 1
    confidence: 0.2
  P2293:
    value: Q18049203
    source count: 1
    confidence: 0.2
    value label: NUS1
  P2888:
    value: http://purl.obolibrary.org/obo/DOID_0080227
    source count: 1
    confidence: 0.2
  P2888:
    value: http://www.orpha.net/ORDO/Orphanet_442835
    source count: 0
    confidence: 0.0
  P5008:
    value: Q4099686
    source count: 0
    confidence: 0.0
    value label: WikiProject Medicine
  P5270:
    value: MONDO_0030921
    source count: 0
    confidence: 0.0
  P11430:
    value: DI-05178
    source count: 0
    confidence: 0.0
citations:
  source: Disease Ontology
  stated in qid: Q5282129
  retrieved: 2019-05-15
citations:
  source: Monarch Disease Ontology release 2018-06-29
  stated in qid: Q55345445
  retrieved: 2018-08-07
citations:
  source: UniProt
  stated in qid: Q905695
  retrieved: 2019-08-13
meta:
  wikidata id: Q53660475
  domain: class_of_disease
  level: standard
  html url: https://4ort.xyz/entity/autosomal-dominant-mental-retardation-55
  markdown url: https://4ort.xyz/entity/autosomal-dominant-mental-retardation-55.md
  facts url summary: https://4ort.xyz/entity/autosomal-dominant-mental-retardation-55/facts.json
  facts url standard: https://4ort.xyz/entity/autosomal-dominant-mental-retardation-55/facts.json
  facts url full: https://4ort.xyz/entity/autosomal-dominant-mental-retardation-55/facts.json
  data source: Wikidata (CC0 / public domain)
  license: https://creativecommons.org/publicdomain/zero/1.0/
  api version: v1
  served at: 2026-08-02T05:31:26.745073Z
  entity updated at: 2026-05-03T22:54:58.348740+00:00Z
  entity created at: 2026-05-03T14:44:12.717693+00:00Z