hawkinsinuria
type: Thing
description: disease
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: tyrosinemia
additional property: PropertyValue
  property ID: P279
  value: amino acid metabolic disorder
additional property: PropertyValue
  property ID: P279
  value: autosomal dominant disease
additional property: PropertyValue
  property ID: P486
  value: C535845
additional property: PropertyValue
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additional property: PropertyValue
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additional property: PropertyValue
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additional property: PropertyValue
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additional property: PropertyValue
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  value: endocrinology
additional property: PropertyValue
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additional property: PropertyValue
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additional property: PropertyValue
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additional property: PropertyValue
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additional property: PropertyValue
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additional property: PropertyValue
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additional property: PropertyValue
  property ID: P6366
  value: 2910486787
additional property: PropertyValue
  property ID: P11143
  value: Hawkinsinuria
additional property: PropertyValue
  property ID: P11430
  value: DI-00540
confidence:
  popularity graph score:
    score: 0.001
    score pct: 0
    tier: established
    components:
      sitelinks: 0
      sitelinks norm: 0.0
      unique citations: 5
      unique citations norm: 0.002
      monthly pageviews: 0
      monthly pageviews norm: 0.0
  sitelinks: 0
  unique citations: 5
  monthly pageviews: 0
  yearly pageviews: 39
  pageview trend:
    m: 2026-06
    v: 31
  pageview trend:
    m: 2026-05
    v: 8
  tier: established
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: Q1122668
    source count: 1
    confidence: 0.2
    value label: tyrosinemia
  P279:
    value: Q18558086
    source count: 1
    confidence: 0.2
    value label: amino acid metabolic disorder
  P279:
    value: Q18553439
    source count: 1
    confidence: 0.2
    value label: autosomal dominant disease
  P486:
    value: C535845
    source count: 1
    confidence: 0.2
  P492:
    value: 140350
    source count: 2
    confidence: 0.4
  P494:
    value: E72.1
    source count: 1
    confidence: 0.2
  P557:
    value: 29836
    source count: 1
    confidence: 0.2
  P699:
    value: DOID:0111362
    source count: 1
    confidence: 0.2
  P1550:
    value: 2118
    source count: 1
    confidence: 0.2
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    value: Q162606
    source count: 0
    confidence: 0.0
    value label: endocrinology
  P2293:
    value: Q18027235
    source count: 2
    confidence: 0.4
    value label: HPD
  P2888:
    value: http://www.orpha.net/ORDO/Orphanet_2118
    source count: 0
    confidence: 0.0
  P2888:
    value: http://purl.obolibrary.org/obo/DOID_0111362
    source count: 1
    confidence: 0.2
  P2888:
    value: http://identifiers.org/doid/DOID:0111362
    source count: 1
    confidence: 0.2
  P2892:
    value: C2931042
    source count: 1
    confidence: 0.2
  P4229:
    value: E70.2
    source count: 1
    confidence: 0.2
  P4317:
    value: 5668
    source count: 1
    confidence: 0.2
  P5270:
    value: MONDO_0007700
    source count: 0
    confidence: 0.0
  P6366:
    value: 2777403441
    source count: 0
    confidence: 0.0
  P6366:
    value: 2910486787
    source count: 0
    confidence: 0.0
  P11143:
    value: Hawkinsinuria
    source count: 0
    confidence: 0.0
  P11430:
    value: DI-00540
    source count: 0
    confidence: 0.0

source: Open Targets Platform
stated in qid: Q113138000
retrieved: 2023-08-24

source: Identifiers.org
stated in qid: Q16335166

source: Monarch Disease Ontology release 2018-06-29
stated in qid: Q55345445
retrieved: 2018-07-28

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

source: Mutations in the 4-hydroxyphenylpyruvic acid dioxygenase gene are responsible for tyrosinemia type III and hawkinsinuria
stated in qid: Q28143604

wikidata id: Q5685180
domain: rare_disease
level: standard
html url: https://4ort.xyz/entity/hawkinsinuria
markdown url: https://4ort.xyz/entity/hawkinsinuria.md
facts url summary: https://4ort.xyz/entity/hawkinsinuria/facts.json
facts url standard: https://4ort.xyz/entity/hawkinsinuria/facts.json
facts url full: https://4ort.xyz/entity/hawkinsinuria/facts.json
data source: Wikidata (CC0 / public domain)
license: https://creativecommons.org/publicdomain/zero/1.0/
api version: v1
served at: 2026-08-24T10:06:31.866747Z
entity updated at: 2026-05-03T21:19:00.258443+00:00Z
entity created at: 2026-05-03T15:22:15.493125+00:00Z