beta-ketothiolase deficiency

Human disease
MedicalCondition designated_intractable_rare_disease Q4897218
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beta-ketothiolase deficiency

Summary

beta-ketothiolase deficiency is a designated intractable/rare disease[1]. It draws 27 Wikipedia views per month (designated_intractable_rare_disease category, ranking #155 of 201).[2]

Key Facts

  • beta-ketothiolase deficiency's instance of is recorded as designated intractable/rare disease[3].
  • beta-ketothiolase deficiency's instance of is recorded as rare disease[4].
  • beta-ketothiolase deficiency's instance of is recorded as class of disease[5].
  • beta-ketothiolase deficiency is a type of autosomal recessive disease[6].
  • beta-ketothiolase deficiency is a type of congenital disorder of amino acid metabolism[7].
  • beta-ketothiolase deficiency is a type of inborn disorder of ketolysis[8].
  • beta-ketothiolase deficiency is a type of classic organic aciduria[9].
  • beta-ketothiolase deficiency is a type of amino acid metabolic disorder[10].
  • beta-ketothiolase deficiency's external data available at URL is recorded as http://www.nanbyou.or.jp/entry/5443[11].
  • beta-ketothiolase deficiency's NCI Thesaurus ID is recorded as C98841[12].
  • beta-ketothiolase deficiency's genetic association is recorded as ACAT1[13].
  • beta-ketothiolase deficiency's exact match is recorded as http://purl.obolibrary.org/obo/DOID_14723[14].
  • beta-ketothiolase deficiency's exact match is recorded as http://identifiers.org/doid/DOID:14723[15].
  • beta-ketothiolase deficiency's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_134[16].
  • beta-ketothiolase deficiency's on focus list of Wikimedia project is recorded as WikiProject Medicine[17].

Why It Matters

beta-ketothiolase deficiency draws 27 Wikipedia views per month (designated_intractable_rare_disease category, ranking #155 of 201).[2] It has Wikipedia articles in 5 language editions, a strong signal of global cultural recognition.[18] It is known by 24 alternative names across languages and contexts.[19]

References

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

Direct Wikidata claims

  1. [3] . ddrare.nibiohn.go.jp. Retrieved . ddrare.nibiohn.go.jp. Provenance: wikidata.org.
  2. [4] . wikidata.org.
  3. [5] . wikidata.org.
  4. [6] . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  5. [7] . wikidata.org.
  6. [8] . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  7. [9] . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  8. [10] . Disease Ontology. Retrieved . wikidata.org.
  9. [11] . ddrare.nibiohn.go.jp. Retrieved . ddrare.nibiohn.go.jp. Provenance: wikidata.org.
  10. [12] . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  11. [13] . Q905695. Retrieved . search.clinicalgenome.org. Provenance: wikidata.org.
  12. [14] . Disease Ontology. Retrieved . wikidata.org.
  13. [15] . Identifiers.org. registry.identifiers.org. Provenance: wikidata.org.
  14. [16] . wikidata.org.
  15. [17] . wikidata.org.

Class ancestry

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

Aggregate / graph-position facts

  1. [2] . Wikimedia Foundation. dumps.wikimedia.org.
  2. [18] . Wikidata sitelinks. wikidata.org.
  3. [19] . 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). beta-ketothiolase deficiency. Retrieved May 3, 2026, from https://4ort.xyz/entity/beta-ketothiolase-deficiency
MLA “beta-ketothiolase deficiency.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/beta-ketothiolase-deficiency.
BibTeX @misc{4ortxyz_beta-ketothiolase-deficiency_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{beta-ketothiolase deficiency}}, year = {2026}, url = {https://4ort.xyz/entity/beta-ketothiolase-deficiency}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): beta-ketothiolase deficiency — https://4ort.xyz/entity/beta-ketothiolase-deficiency (retrieved 2026-05-03)

Canonical URL: https://4ort.xyz/entity/beta-ketothiolase-deficiency · Last refreshed:

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. 10w ago · JhealdBatch bot · 2026-07-05 view diff on Wikidata ↗
    On focus list of wikimedia project WikiProject Medicine
    Subclass of autosomal recessive disease, congenital disorder of amino acid metabolism, inborn disorder of ketolysis +2
    Subclass of
    Genetic association ACAT1
    + 3 other properties edited (see Wikidata diff for full list)
    "/* wbeditentity-update:0| */ QuickStatements 3.0 [[:toollabs:qs-dev/batch/39953|batch #39953]]: deprecate redundant disease superclasses (2)"
Live feed via Wikidata EventStreams. New edits appear within minutes of being made on Wikidata.