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coenzyme Q10 deficiency, primary, 8; COQ10D8

human disease
MedicalCondition developmental_defect_during_embryogenesis Q55784979
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Summary

coenzyme Q10 deficiency, primary, 8; COQ10D8 is a developmental defect during embryogenesis[1]. It is known by 5 alternative names across languages and contexts.[2]

Key Facts

  • Instance of: rare disease[3], disease[4], class of disease[5]
  • Subclass of: coenzyme Q10 deficiency disease[6], genetic disease[7]
  • Genetic association: COQ7[8]
  • Exact match: http://purl.obolibrary.org/obo/DOID_0070245[9], http://identifiers.org/doid/DOID:0070245[10]
  • On focus list of Wikimedia project: WikiProject Medicine[11]

References

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

Direct Wikidata claims

  1. [3] ↑ . wikidata.org.
  2. [4] ↑ . Rescue of primary ubiquinone deficiency due to a novel COQ7 defect using 2,4-dihydroxybensoic acid.. wikidata.org.
  3. [5] ↑ . wikidata.org.
  4. [6] ↑ . Disease Ontology. Retrieved . wikidata.org.
  5. [7] ↑ . Disease Ontology. Retrieved . wikidata.org.
  6. [8] ↑ . UniProt. Retrieved . wikidata.org.
  7. [9] ↑ . Disease Ontology. Retrieved . wikidata.org.
  8. [10] ↑ . Identifiers.org. registry.identifiers.org. Provenance: wikidata.org.
  9. [11] ↑ . wikidata.org.

Class ancestry

  1. [1] ↑ . Wikidata. wikidata.org.

Aggregate / graph-position facts

  1. [2] ↑ . 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). coenzyme Q10 deficiency, primary, 8; COQ10D8. Retrieved May 3, 2026, from https://4ort.xyz/entity/coenzyme-q10-deficiency-primary-8-coq10d8
MLA “coenzyme Q10 deficiency, primary, 8; COQ10D8.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/coenzyme-q10-deficiency-primary-8-coq10d8.
BibTeX @misc{4ortxyz_coenzyme-q10-deficiency-primary-8-coq10d8_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{coenzyme Q10 deficiency, primary, 8; COQ10D8}}, year = {2026}, url = {https://4ort.xyz/entity/coenzyme-q10-deficiency-primary-8-coq10d8}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): coenzyme Q10 deficiency, primary, 8; COQ10D8 — https://4ort.xyz/entity/coenzyme-q10-deficiency-primary-8-coq10d8 (retrieved 2026-05-03)

Canonical URL: https://4ort.xyz/entity/coenzyme-q10-deficiency-primary-8-coq10d8 · 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. 15w ago · JhealdBatch bot · 2026-07-05 view diff on Wikidata ↗
    Subclass of → coenzyme Q10 deficiency disease, genetic disease
    Instance of → developmental defect during embryogenesis, rare disease, disease +1
    "/* wbeditentity-update:0| */ QuickStatements 3.0 [[:toollabs:qs-dev/batch/39943|batch #39943]]: deprecate redundant disease superclasses"
  2. 16w ago · JhealdBatch bot · 2026-07-03 view diff on Wikidata ↗
    Mondo id → MONDO_0014754
    Genetic association → COQ7
    Instance of → developmental defect during embryogenesis, rare disease, disease +1
    Imported from → —
    + 8 other properties edited (see Wikidata diff for full list)
    "/* wbeditentity-update:0| */ QuickStatements 3.0 [[:toollabs:qs-dev/batch/39731|batch #39731]]: rm redundant P31"
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