Nestor-Guillermo progeria syndrome

human disease
MedicalCondition developmental_defect_during_embryogenesis Q55784059
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Summary

Nestor-Guillermo progeria syndrome is a developmental defect during embryogenesis[1]. It draws 37 Wikipedia views per month (developmental defect during embryogenesis category, ranking #135 of 308).[2]

Key Facts

  • Instance of: rare disease[3], class of disease[4]
  • Subclass of: progeria[5]
  • Genetic association: BANF1[6]
  • Exact match: http://www.orpha.net/ORDO/Orphanet_280576[7]

Why It Matters

Nestor-Guillermo progeria syndrome is known by 6 alternative names across languages and contexts.[8]

📑 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). Nestor-Guillermo progeria syndrome. Retrieved October 22, 2026, from https://4ort.xyz/entity/nestor-guillermo-progeria-syndrome
MLA “Nestor-Guillermo progeria syndrome.” 4ort.xyz Knowledge Graph, 4ort.xyz, 22 Oct. 2026, https://4ort.xyz/entity/nestor-guillermo-progeria-syndrome.
BibTeX @misc{4ortxyz_nestor-guillermo-progeria-syndrome_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{Nestor-Guillermo progeria syndrome}}, year = {2026}, url = {https://4ort.xyz/entity/nestor-guillermo-progeria-syndrome}, note = {Accessed: 2026-10-22}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): Nestor-Guillermo progeria syndrome — https://4ort.xyz/entity/nestor-guillermo-progeria-syndrome (retrieved 2026-10-22)

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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. 15w ago · JhealdBatch bot · 2026-07-03 view diff on Wikidata ↗
    Mondo id → MONDO_0013523
    Genetic association → BANF1
    Gard rare disease id → 11008
    Orphanet id → 280576
    + 11 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"
Live feed via Wikidata EventStreams. New edits appear within minutes of being made on Wikidata.