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Lipoyl transferase 1 deficiency

human disease
MedicalCondition developmental_defect_during_embryogenesis Q55784889
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Summary

Lipoyl transferase 1 deficiency is a developmental defect during embryogenesis[1]. It is known by 4 alternative names across languages and contexts.[2]

Key Facts

  • Instance of: rare disease[3], class of disease[4]
  • Subclass of: lipoic acid biosynthesis defect[5]
  • Genetic association: LIPT1[6]
  • Exact match: http://www.orpha.net/ORDO/Orphanet_401862[7]

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] ↑ . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  4. [6] ↑ . UniProt. Retrieved . platform.opentargets.org. Provenance: wikidata.org.
  5. [7] ↑ . 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). Lipoyl transferase 1 deficiency. Retrieved May 3, 2026, from https://4ort.xyz/entity/lipoyl-transferase-1-deficiency
MLA “Lipoyl transferase 1 deficiency.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/lipoyl-transferase-1-deficiency.
BibTeX @misc{4ortxyz_lipoyl-transferase-1-deficiency_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{Lipoyl transferase 1 deficiency}}, year = {2026}, url = {https://4ort.xyz/entity/lipoyl-transferase-1-deficiency}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): Lipoyl transferase 1 deficiency — https://4ort.xyz/entity/lipoyl-transferase-1-deficiency (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. 14w ago · JhealdBatch bot · 2026-07-03 view diff on Wikidata ↗
    Mondo id → MONDO_0014576
    Genetic association → LIPT1
    Orphanet id → 401862
    Instance of → developmental defect during embryogenesis, rare disease, class of disease
    + 8 other properties edited (see Wikidata diff for full list)
    "/* wbeditentity-update:0| */ QuickStatements 3.0 [[:toollabs:qs-dev/batch/39742|batch #39742]]: subclass of disease, not instance"
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