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Lathosterolosis

Lathosterolosis is an extremely rare inborn error of sterol biosynthesis characterized by facial dysmorphism, congenital anomalies (including limb and kidney anomalies), failure to thrive, developmental delay and liver disease
MedicalCondition developmental_defect_during_embryogenesis Q6495941
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Lathosterolosis

Summary

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

Key Facts

  • Lathosterolosis's instance of is recorded as developmental defect during embryogenesis[3].
  • Lathosterolosis's instance of is recorded as rare disease[4].
  • Lathosterolosis's instance of is recorded as class of disease[5].
  • Lathosterolosis is a type of sterol biosynthesis disorder[6].
  • Lathosterolosis's genetic association is recorded as SC5D[7].
  • Lathosterolosis's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_46059[8].

Why It Matters

Lathosterolosis is known by 4 alternative names across languages and contexts.[2]

References

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

Direct Wikidata claims

  1. [3] ↑ . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  2. [4] ↑ . wikidata.org.
  3. [5] ↑ . wikidata.org.
  4. [6] ↑ . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  5. [7] ↑ . Q905695. Retrieved . platform.opentargets.org. Provenance: wikidata.org.
  6. [8] ↑ . wikidata.org.

Class ancestry

  1. [1] ↑ . Wikidata. wikidata.org.

Aggregate / graph-position facts

  1. [2] ↑ . Wikidata aliases. wikidata.org.

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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). Lathosterolosis. Retrieved May 3, 2026, from https://4ort.xyz/entity/lathosterolosis
MLA “Lathosterolosis.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/lathosterolosis.
BibTeX @misc{4ortxyz_lathosterolosis_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{Lathosterolosis}}, year = {2026}, url = {https://4ort.xyz/entity/lathosterolosis}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): Lathosterolosis — https://4ort.xyz/entity/lathosterolosis (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. 10w ago · JhealdBatch bot · 2026-07-03 view diff on Wikidata ↗
    Mondo id → MONDO_0011816
    Genetic association → SC5D
    Gard rare disease id → 9711
    Orphanet id → 46059
    + 12 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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