multiple acyl-CoA dehydrogenase deficiency

medical condition
MedicalCondition designated_intractable_rare_disease Q1403045
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multiple acyl-CoA dehydrogenase deficiency

Summary

multiple acyl-CoA dehydrogenase deficiency is a designated intractable/rare disease[1]. It has Wikipedia articles in 5 language editions, a strong signal of global cultural recognition.[2]

Key Facts

  • multiple acyl-CoA dehydrogenase deficiency's instance of is recorded as designated intractable/rare disease[3].
  • multiple acyl-CoA dehydrogenase deficiency's instance of is recorded as class of disease[4].
  • multiple acyl-CoA dehydrogenase deficiency is a type of inherited metabolic disorder[5].
  • multiple acyl-CoA dehydrogenase deficiency is a type of acyl-CoA dehydrogenase deficiency[6].
  • multiple acyl-CoA dehydrogenase deficiency is a type of fatty acid oxidation and ketogenesis disorder with hypertrophic cardiomyopathy[7].
  • multiple acyl-CoA dehydrogenase deficiency is a type of genetic disease[8].
  • multiple acyl-CoA dehydrogenase deficiency is a type of glutaric aciduria[9].
  • multiple acyl-CoA dehydrogenase deficiency's external data available at URL is recorded as http://www.nanbyou.or.jp/entry/4819[10].
  • multiple acyl-CoA dehydrogenase deficiency's NCI Thesaurus ID is recorded as C99102[11].
  • multiple acyl-CoA dehydrogenase deficiency's NCI Thesaurus ID is recorded as C84907[12].
  • multiple acyl-CoA dehydrogenase deficiency's health specialty is recorded as medical genetics[13].
  • multiple acyl-CoA dehydrogenase deficiency's health specialty is recorded as endocrinology[14].
  • multiple acyl-CoA dehydrogenase deficiency's genetic association is recorded as ETFB[15].
  • multiple acyl-CoA dehydrogenase deficiency's genetic association is recorded as ETFA[16].
  • multiple acyl-CoA dehydrogenase deficiency's genetic association is recorded as ETFDH[17].
  • multiple acyl-CoA dehydrogenase deficiency's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0060358[18].
  • multiple acyl-CoA dehydrogenase deficiency's exact match is recorded as http://identifiers.org/doid/DOID:0060358[19].
  • multiple acyl-CoA dehydrogenase deficiency's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_26791[20].
  • multiple acyl-CoA dehydrogenase deficiency's on focus list of Wikimedia project is recorded as WikiProject Medicine[21].

Why It Matters

multiple acyl-CoA dehydrogenase deficiency has Wikipedia articles in 5 language editions, a strong signal of global cultural recognition.[2] It is known by 24 alternative names across languages and contexts.[22]

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] ↑ . Disease Ontology. Retrieved . wikidata.org.
  4. [6] ↑ . Monarch Disease Ontology release 2018-06-29. Retrieved . 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] ↑ . ddrare.nibiohn.go.jp. Retrieved . ddrare.nibiohn.go.jp. Provenance: wikidata.org.
  9. [11] ↑ . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  10. [12] ↑ . Disease Ontology. Retrieved . wikidata.org.
  11. [13] ↑ . wikidata.org.
  12. [14] ↑ . wikidata.org.
  13. [15] ↑ . Q905695. Retrieved . platform.opentargets.org. Provenance: wikidata.org.
  14. [16] ↑ . Q905695. Retrieved . search.clinicalgenome.org. Provenance: wikidata.org.
  15. [17] ↑ . Q905695. Retrieved . search.clinicalgenome.org. Provenance: wikidata.org.
  16. [18] ↑ . Disease Ontology. Retrieved . wikidata.org.
  17. [19] ↑ . Identifiers.org. registry.identifiers.org. Provenance: wikidata.org.
  18. [20] ↑ . wikidata.org.
  19. [21] ↑ . wikidata.org.

Class ancestry

  1. [1] ↑ . Wikidata. wikidata.org.

Aggregate / graph-position facts

  1. [2] ↑ . Wikidata sitelinks. wikidata.org.
  2. [22] ↑ . 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). multiple acyl-CoA dehydrogenase deficiency. Retrieved October 5, 2026, from https://4ort.xyz/entity/multiple-acyl-coa-dehydrogenase-deficiency
MLA “multiple acyl-CoA dehydrogenase deficiency.” 4ort.xyz Knowledge Graph, 4ort.xyz, 5 Oct. 2026, https://4ort.xyz/entity/multiple-acyl-coa-dehydrogenase-deficiency.
BibTeX @misc{4ortxyz_multiple-acyl-coa-dehydrogenase-deficiency_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{multiple acyl-CoA dehydrogenase deficiency}}, year = {2026}, url = {https://4ort.xyz/entity/multiple-acyl-coa-dehydrogenase-deficiency}, note = {Accessed: 2026-10-05}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): multiple acyl-CoA dehydrogenase deficiency — https://4ort.xyz/entity/multiple-acyl-coa-dehydrogenase-deficiency (retrieved 2026-10-05)

Canonical URL: https://4ort.xyz/entity/multiple-acyl-coa-dehydrogenase-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. 13w ago · JhealdBatch bot · 2026-07-05 view diff on Wikidata ↗
    On focus list of wikimedia project → WikiProject Medicine
    Health specialty → medical genetics, endocrinology
    Subclass of → inherited metabolic disorder, acyl-CoA dehydrogenase deficiency, fatty acid oxidation and ketogenesis disorder with hypertrophic cardiomyopathy +2
    Subclass of → —
    + 4 other properties edited (see Wikidata diff for full list)
    "/* wbeditentity-update:0| */ QuickStatements 3.0 [[:toollabs:qs-dev/batch/39943|batch #39943]]: deprecate redundant disease superclasses"
Live feed via Wikidata EventStreams. New edits appear within minutes of being made on Wikidata.