Usher syndrome type 1
type: Thing
description: Usher syndrome characterized by profound congenital deafness, vestibular dysfunction and early development of retinitis pigmentosa
additional property: PropertyValue
  property ID: P31
  value: class of disease
additional property: PropertyValue
  property ID: P279
  value: Usher syndrome
additional property: PropertyValue
  property ID: P492
  value: 276900
additional property: PropertyValue
  property ID: P699
  value: DOID:0110826
additional property: PropertyValue
  property ID: P1550
  value: 231169
additional property: PropertyValue
  property ID: P1748
  value: C126327
additional property: PropertyValue
  property ID: P2888
  value: http://purl.obolibrary.org/obo/DOID_0110826
additional property: PropertyValue
  property ID: P2888
  value: http://identifiers.org/doid/DOID:0110826
additional property: PropertyValue
  property ID: P2888
  value: http://www.orpha.net/ORDO/Orphanet_231169
additional property: PropertyValue
  property ID: P2892
  value: C0339533
additional property: PropertyValue
  property ID: P4229
  value: H35.5
additional property: PropertyValue
  property ID: P4317
  value: 5435
additional property: PropertyValue
  property ID: P5008
  value: WikiProject Medicine
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: 0
      monthly pageviews norm: 0.0
  sitelinks: 0
  unique citations: 2
  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: Q917399
    source count: 1
    confidence: 0.2
    value label: Usher syndrome
  P492:
    value: 276900
    source count: 1
    confidence: 0.2
  P699:
    value: DOID:0110826
    source count: 1
    confidence: 0.2
  P1550:
    value: 231169
    source count: 1
    confidence: 0.2
  P1748:
    value: C126327
    source count: 0
    confidence: 0.0
  P2888:
    value: http://purl.obolibrary.org/obo/DOID_0110826
    source count: 1
    confidence: 0.2
  P2888:
    value: http://identifiers.org/doid/DOID:0110826
    source count: 1
    confidence: 0.2
  P2888:
    value: http://www.orpha.net/ORDO/Orphanet_231169
    source count: 0
    confidence: 0.0
  P2892:
    value: C0339533
    source count: 1
    confidence: 0.2
  P4229:
    value: H35.5
    source count: 1
    confidence: 0.2
  P4317:
    value: 5435
    source count: 0
    confidence: 0.0
  P5008:
    value: Q4099686
    source count: 0
    confidence: 0.0
    value label: WikiProject Medicine
citations:
  source: Identifiers.org
  stated in qid: Q16335166
citations:
  source: Disease Ontology
  stated in qid: Q5282129
  retrieved: 2020-11-30
meta:
  wikidata id: Q32143464
  domain: class_of_disease
  level: standard
  html url: https://4ort.xyz/entity/usher-syndrome-type-1
  markdown url: https://4ort.xyz/entity/usher-syndrome-type-1.md
  facts url summary: https://4ort.xyz/entity/usher-syndrome-type-1/facts.json
  facts url standard: https://4ort.xyz/entity/usher-syndrome-type-1/facts.json
  facts url full: https://4ort.xyz/entity/usher-syndrome-type-1/facts.json
  data source: Wikidata (CC0 / public domain)
  license: https://creativecommons.org/publicdomain/zero/1.0/
  api version: v1
  served at: 2026-08-24T22:36:21.202033Z
  entity updated at: 2026-05-03T22:54:58.348740+00:00Z
  entity created at: 2026-05-03T14:27:06.273395+00:00Z