dystrophic epidermolysis bullosa pruriginosa

Dystrophic epidermolysis bullosa pruriginosa is a rare subtype of dystrophic epidermolysis bullosa (DEB, see this term) characterized by generalized or localized skin lesions associated with severe, if not intractable, pruritus
MedicalCondition developmental_defect_during_embryogenesis Q55783353
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dystrophic epidermolysis bullosa pruriginosa

Summary

dystrophic epidermolysis bullosa pruriginosa is a developmental defect during embryogenesis[1].

Key Facts

  • dystrophic epidermolysis bullosa pruriginosa's instance of is recorded as developmental defect during embryogenesis[2].
  • dystrophic epidermolysis bullosa pruriginosa's instance of is recorded as rare disease[3].
  • dystrophic epidermolysis bullosa pruriginosa's instance of is recorded as class of disease[4].
  • dystrophic epidermolysis bullosa pruriginosa is a type of epidermolysis bullosa dystrophica[5].
  • dystrophic epidermolysis bullosa pruriginosa's ICD-9-CM is recorded as 757.39[6].
  • dystrophic epidermolysis bullosa pruriginosa's genetic association is recorded as COL7A1[7].
  • dystrophic epidermolysis bullosa pruriginosa's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_89843[8].

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APA 4ort.xyz Knowledge Graph. (2026). dystrophic epidermolysis bullosa pruriginosa. Retrieved May 3, 2026, from https://4ort.xyz/entity/dystrophic-epidermolysis-bullosa-pruriginosa
MLA “dystrophic epidermolysis bullosa pruriginosa.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/dystrophic-epidermolysis-bullosa-pruriginosa.
BibTeX @misc{4ortxyz_dystrophic-epidermolysis-bullosa-pruriginosa_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{dystrophic epidermolysis bullosa pruriginosa}}, year = {2026}, url = {https://4ort.xyz/entity/dystrophic-epidermolysis-bullosa-pruriginosa}, note = {Accessed: 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. 8d ago · JhealdBatch bot · 2026-07-03 view diff on Wikidata ↗
    Mondo id MONDO_0011398
    Genetic association COL7A1
    Orphanet id 89843
    Instance of developmental defect during embryogenesis, rare disease, class of disease
    + 9 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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