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Fitzsimmons–Guilbert syndrome

medical condition
MedicalCondition developmental_defect_during_embryogenesis Q5455731
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Fitzsimmons–Guilbert syndrome

Summary

Fitzsimmons–Guilbert syndrome is a developmental defect during embryogenesis[1]. It draws 19 Wikipedia views per month (developmental_defect_during_embryogenesis category, ranking #133 of 308).[2]

Key Facts

  • Fitzsimmons–Guilbert syndrome's instance of is recorded as developmental defect during embryogenesis[3].
  • Fitzsimmons–Guilbert syndrome's instance of is recorded as class of disease[4].
  • Fitzsimmons–Guilbert syndrome is a type of hereditary spastic paraplegia[5].
  • Fitzsimmons–Guilbert syndrome is a type of syndrome with brachydactyly[6].
  • Fitzsimmons–Guilbert syndrome is a type of genetic nervous system disorder[7].
  • Fitzsimmons–Guilbert syndrome's symptoms and signs is recorded as brachydactyly[8].
  • Fitzsimmons–Guilbert syndrome's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_2823[9].

Why It Matters

Fitzsimmons–Guilbert syndrome draws 19 Wikipedia views per month (developmental_defect_during_embryogenesis category, ranking #133 of 308).[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] ↑ . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  6. [8] ↑ . wikidata.org.
  7. [9] ↑ . wikidata.org.

Class ancestry

  1. [1] ↑ . Wikidata. wikidata.org.

Aggregate / graph-position facts

  1. [2] ↑ . Wikimedia Foundation. dumps.wikimedia.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). Fitzsimmons–Guilbert syndrome. Retrieved May 3, 2026, from https://4ort.xyz/entity/fitzsimmons-guilbert-syndrome
MLA “Fitzsimmons–Guilbert syndrome.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/fitzsimmons-guilbert-syndrome.
BibTeX @misc{4ortxyz_fitzsimmons-guilbert-syndrome_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{Fitzsimmons–Guilbert syndrome}}, year = {2026}, url = {https://4ort.xyz/entity/fitzsimmons-guilbert-syndrome}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): Fitzsimmons–Guilbert syndrome — https://4ort.xyz/entity/fitzsimmons-guilbert-syndrome (retrieved 2026-05-03)

Canonical URL: https://4ort.xyz/entity/fitzsimmons-guilbert-syndrome · 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. 4w ago · JhealdBatch bot · 2026-07-03 view diff on Wikidata ↗
    Mondo id → MONDO_0010045
    Orphanet id → 2823
    Instance of → developmental defect during embryogenesis, class of disease
    Imported from → —
    + 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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