trichothiodystrophy 3, photosensitive

human disease
MedicalCondition developmental_defect_during_embryogenesis Q55784902
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trichothiodystrophy 3, photosensitive

Summary

trichothiodystrophy 3, photosensitive is a developmental defect during embryogenesis[1].

Key Facts

  • trichothiodystrophy 3, photosensitive's instance of is recorded as developmental defect during embryogenesis[2].
  • trichothiodystrophy 3, photosensitive's instance of is recorded as class of disease[3].
  • trichothiodystrophy 3, photosensitive is a type of trichothiodystrophy syndromes[4].
  • trichothiodystrophy 3, photosensitive is a type of autosomal recessive disease[5].
  • trichothiodystrophy 3, photosensitive's NCI Thesaurus ID is recorded as C173099[6].
  • trichothiodystrophy 3, photosensitive's genetic association is recorded as GTF2H5[7].
  • trichothiodystrophy 3, photosensitive's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0111871[8].
  • trichothiodystrophy 3, photosensitive's exact match is recorded as http://identifiers.org/doid/DOID:0111871[9].

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APA 4ort.xyz Knowledge Graph. (2026). trichothiodystrophy 3, photosensitive. Retrieved May 3, 2026, from https://4ort.xyz/entity/trichothiodystrophy-3-photosensitive
MLA “trichothiodystrophy 3, photosensitive.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/trichothiodystrophy-3-photosensitive.
BibTeX @misc{4ortxyz_trichothiodystrophy-3-photosensitive_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{trichothiodystrophy 3, photosensitive}}, year = {2026}, url = {https://4ort.xyz/entity/trichothiodystrophy-3-photosensitive}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): trichothiodystrophy 3, photosensitive — https://4ort.xyz/entity/trichothiodystrophy-3-photosensitive (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. 16d ago · JhealdBatch bot · 2026-07-03 view diff on Wikidata ↗
    Mondo id MONDO_0014619
    Genetic association GTF2H5
    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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