tyrosinemia type I

tyrosinemia that has material basis in deficiency of the enzyme fumarylacetoacetate hydrolase resulting in an increase in fumarylacetoacetate which inhibits previous steps in tyrosine degradation leading to an accumulation of tyrosine in the body
MedicalCondition rare_disease Q1747726
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tyrosinemia type I

Summary

tyrosinemia type I is a rare disease[1]. It draws 32 Wikipedia views per month (rare_disease category, ranking #218 of 627).[2]

Key Facts

  • tyrosinemia type I's instance of is recorded as rare disease[3].
  • tyrosinemia type I's instance of is recorded as designated intractable/rare disease[4].
  • tyrosinemia type I's instance of is recorded as class of disease[5].
  • tyrosinemia type I's subclass of is recorded as tyrosinemia[6].
  • tyrosinemia type I's OMIM ID is recorded as 276700[7].
  • tyrosinemia type I's ICD-9 ID is recorded as 270.2[8].
  • tyrosinemia type I's ICD-10 ID is recorded as E70.2[9].
  • tyrosinemia type I's DiseasesDB is recorded as 13478[10].
  • tyrosinemia type I's Freebase ID is recorded as /m/047lb98[11].
  • tyrosinemia type I's Disease Ontology ID is recorded as DOID:0050726[12].
  • tyrosinemia type I's Orphanet ID is recorded as 882[13].
  • tyrosinemia type I's NCI Thesaurus ID is recorded as C98641[14].
  • tyrosinemia type I's health specialty is recorded as endocrinology[15].
  • tyrosinemia type I's genetic association is recorded as FAH[16].
  • tyrosinemia type I's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0050726[17].
  • tyrosinemia type I's exact match is recorded as http://identifiers.org/doid/DOID:0050726[18].
  • tyrosinemia type I's PatientsLikeMe condition ID is recorded as tyrosinemia-type-i[19].
  • tyrosinemia type I's GARD rare disease ID is recorded as 2658[20].
  • tyrosinemia type I's on focus list of Wikimedia project is recorded as WikiProject Medicine[21].
  • tyrosinemia type I's Mondo ID is recorded as MONDO_0010161[22].
  • tyrosinemia type I's Microsoft Academic ID is recorded as 2776022542[23].
  • tyrosinemia type I's has phenotype is recorded as Hypertyrosinemia[24].
  • tyrosinemia type I's ICD-11 ID is recorded as 5C50.11[25].
  • tyrosinemia type I's ICD-11 ID is recorded as 2029519782[26].
  • tyrosinemia type I's WikiProjectMed ID is recorded as Tyrosinemia type I[27].

Why It Matters

tyrosinemia type I draws 32 Wikipedia views per month (rare_disease category, ranking #218 of 627).[2] It has Wikipedia articles in 7 language editions, a strong signal of global cultural recognition.[28] It is known by 6 alternative names across languages and contexts.[29]

References

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

Direct Wikidata claims

  1. [3] . wikidata.org.
  2. [4] . wikidata.org.
  3. [5] . wikidata.org.
  4. [6] . Disease Ontology. Retrieved . wikidata.org.
  5. [7] . Disease Ontology. Retrieved . wikidata.org.
  6. [8] . wikidata.org.
  7. [9] . wikidata.org.
  8. [10] . wikidata.org.
  9. [11] . Freebase Data Dumps. wikidata.org.
  10. [12] . Disease Ontology. Retrieved . wikidata.org.
  11. [13] . wikidata.org.
  12. [14] . wikidata.org.
  13. [15] . wikidata.org.
  14. [16] . A single mutation of the fumarylacetoacetate hydrolase gene in French Canadians with hereditary tyrosinemia type I. Retrieved . platform.opentargets.org. Provenance: wikidata.org.
  15. [17] . Disease Ontology. Retrieved . wikidata.org.
  16. [18] . Identifiers.org. registry.identifiers.org. Provenance: wikidata.org.
  17. [19] . wikidata.org.
  18. [20] . wikidata.org.
  19. [21] . wikidata.org.
  20. [22] . wikidata.org.
  21. [23] . wikidata.org.
  22. [24] . Disease Ontology. Retrieved . wikidata.org.
  23. [25] . wikidata.org.
  24. [26] . wikidata.org.
  25. [27] . wikidata.org.

Class ancestry

  1. [1] . Wikidata. wikidata.org.

Aggregate / graph-position facts

  1. [2] . Wikimedia Foundation. dumps.wikimedia.org.
  2. [28] . Wikidata sitelinks. wikidata.org.
  3. [29] . Wikidata aliases. 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 type I. Retrieved May 3, 2026, from https://4ort.xyz/entity/tyrosinemia-type-i
MLA “tyrosinemia type I.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/tyrosinemia-type-i.
BibTeX @misc{4ortxyz_tyrosinemia-type-i_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{tyrosinemia type I}}, year = {2026}, url = {https://4ort.xyz/entity/tyrosinemia-type-i}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): tyrosinemia type I — https://4ort.xyz/entity/tyrosinemia-type-i (retrieved 2026-05-03)

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