Trevor's disease

Orthopedic disease
MedicalCondition developmental_defect_during_embryogenesis Q7839508
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Trevor's disease

Summary

Trevor's disease is a developmental defect during embryogenesis[1]. It draws 2 Wikipedia views per month (developmental_defect_during_embryogenesis category, ranking #134 of 308).[2]

Key Facts

  • Trevor's disease's instance of is recorded as developmental defect during embryogenesis[3].
  • Trevor's disease's instance of is recorded as class of disease[4].
  • Trevor's disease is a type of primary bone dysplasia with disorganized development of skeletal components[5].
  • Trevor's disease's Commons category is recorded as Trevor's disease[6].
  • Trevor's disease's ICD-9-CM is recorded as 756.59[7].
  • Trevor's disease's health specialty is recorded as medical genetics[8].
  • Trevor's disease's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_1822[9].

Why It Matters

Trevor's disease draws 2 Wikipedia views per month (developmental_defect_during_embryogenesis category, ranking #134 of 308).[2] It is known by 9 alternative names across languages and contexts.[10]

📑 Cite this page

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APA 4ort.xyz Knowledge Graph. (2026). Trevor's disease. Retrieved May 3, 2026, from https://4ort.xyz/entity/trevor-s-disease
MLA “Trevor's disease.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/trevor-s-disease.
BibTeX @misc{4ortxyz_trevor-s-disease_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{Trevor's disease}}, year = {2026}, url = {https://4ort.xyz/entity/trevor-s-disease}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): Trevor's disease — https://4ort.xyz/entity/trevor-s-disease (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. 11w ago · JhealdBatch bot · 2026-07-03 view diff on Wikidata ↗
    Icd-10 id Q74.8
    Mondo id MONDO_0007489
    Gard rare disease id 2019
    Orphanet id 1822
    + 13 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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