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tyrosinemia

amino acid metabolic disorder that involves impaired break down of the amino acid tyrosine
MedicalCondition class_of_disease Q1122668
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tyrosinemia

Summary

tyrosinemia is a class of disease[1]. tyrosinemia has Wikipedia articles in 14 language editions, a strong signal of global cultural recognition.[2]

Key Facts

  • tyrosinemia's instance of is recorded as class of disease[3].
  • tyrosinemia is a type of inborn disorder of phenylalanine or tyrosine metabolism[4].
  • tyrosinemia is a type of amino acid metabolic disorder[5].
  • tyrosinemia is a type of disease[6].
  • tyrosinemia's ICD-9-CM is recorded as 270.2[7].
  • tyrosinemia's NCI Thesaurus ID is recorded as C98640[8].
  • tyrosinemia's health specialty is recorded as medical genetics[9].
  • tyrosinemia's exact match is recorded as http://purl.obolibrary.org/obo/DOID_9275[10].
  • tyrosinemia's exact match is recorded as http://identifiers.org/doid/DOID:9275[11].
  • tyrosinemia's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_284818[12].
  • tyrosinemia's on focus list of Wikimedia project is recorded as WikiProject Medicine[13].

Why It Matters

tyrosinemia has Wikipedia articles in 14 language editions, a strong signal of global cultural recognition.[2]

Related Entities

disease

References

Programmatic citations — every numbered marker resolves to a verifiable graph row below.

Direct Wikidata claims

  1. [3] ↑ . wikidata.org.
  2. [4] ↑ . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  3. [5] ↑ . Disease Ontology. Retrieved . wikidata.org.
  4. [6] ↑ . wikidata.org.
  5. [7] ↑ . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  6. [8] ↑ . Disease Ontology. Retrieved . wikidata.org.
  7. [9] ↑ . wikidata.org.
  8. [10] ↑ . Disease Ontology. Retrieved . wikidata.org.
  9. [11] ↑ . Identifiers.org. registry.identifiers.org. Provenance: wikidata.org.
  10. [12] ↑ . wikidata.org.
  11. [13] ↑ . wikidata.org.

Class ancestry

  1. [1] ↑ . Wikidata. wikidata.org.

Aggregate / graph-position facts

  1. [2] ↑ . Wikidata sitelinks. wikidata.org.

📑 Cite this page

Use these citations when quoting this entity in research, articles, AI prompts, or wherever provenance matters. We aggregate Wikidata + Wikipedia + authoritative open-data sources; the stitched, scored, cross-referenced view is what 4ort.xyz contributes.

APA 4ort.xyz Knowledge Graph. (2026). tyrosinemia. Retrieved May 3, 2026, from https://4ort.xyz/entity/tyrosinemia
MLA “tyrosinemia.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/tyrosinemia.
BibTeX @misc{4ortxyz_tyrosinemia_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{tyrosinemia}}, year = {2026}, url = {https://4ort.xyz/entity/tyrosinemia}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): tyrosinemia — https://4ort.xyz/entity/tyrosinemia (retrieved 2026-05-03)

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Edit History

Rolling log of changes to this entity's Wikidata record. Values shown reflect the current state of each edited property — follow the history link to see the precise diff for any edit.

  1. 7d ago · JhealdBatch bot · 2026-07-03 view diff on Wikidata ↗
    Subclass of → inborn disorder of phenylalanine or tyrosine metabolism, amino acid metabolic disorder, disease
    Health specialty → medical genetics
    Subclass of → —
    Instance of → class of disease
    + 3 other properties edited (see Wikidata diff for full list)
    "/* wbeditentity-update:0| */ QuickStatements 3.0 [[:toollabs:qs-dev/batch/39732|batch #39732]]: rm redundant subclass"
Live feed via Wikidata EventStreams. New edits appear within minutes of being made on Wikidata.