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acroosteolysis-keloid-like lesions-premature aging syndrome

human disease
MedicalCondition developmental_defect_during_embryogenesis Q55783230
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acroosteolysis-keloid-like lesions-premature aging syndrome

Summary

acroosteolysis-keloid-like lesions-premature aging syndrome is a developmental defect during embryogenesis[1].

Key Facts

  • acroosteolysis-keloid-like lesions-premature aging syndrome's instance of is recorded as developmental defect during embryogenesis[2].
  • acroosteolysis-keloid-like lesions-premature aging syndrome's instance of is recorded as rare disease[3].
  • acroosteolysis-keloid-like lesions-premature aging syndrome's instance of is recorded as class of disease[4].
  • acroosteolysis-keloid-like lesions-premature aging syndrome is a type of progeroid syndrome[5].
  • acroosteolysis-keloid-like lesions-premature aging syndrome's genetic association is recorded as PDGFRB[6].
  • acroosteolysis-keloid-like lesions-premature aging syndrome's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_363665[7].

References

Programmatic citations — every numbered marker resolves to a verifiable graph row below.

Direct Wikidata claims

  1. [2] ↑ . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  2. [3] ↑ . wikidata.org.
  3. [4] ↑ . wikidata.org.
  4. [5] ↑ . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  5. [6] ↑ . Q905695. Retrieved . platform.opentargets.org. Provenance: wikidata.org.
  6. [7] ↑ . wikidata.org.

Class ancestry

  1. [1] ↑ . Wikidata. wikidata.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). acroosteolysis-keloid-like lesions-premature aging syndrome. Retrieved May 3, 2026, from https://4ort.xyz/entity/acroosteolysis-keloid-like-lesions-premature-aging-syndrome
MLA “acroosteolysis-keloid-like lesions-premature aging syndrome.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/acroosteolysis-keloid-like-lesions-premature-aging-syndrome.
BibTeX @misc{4ortxyz_acroosteolysis-keloid-like-lesions-premature-aging-syndrome_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{acroosteolysis-keloid-like lesions-premature aging syndrome}}, year = {2026}, url = {https://4ort.xyz/entity/acroosteolysis-keloid-like-lesions-premature-aging-syndrome}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): acroosteolysis-keloid-like lesions-premature aging syndrome — https://4ort.xyz/entity/acroosteolysis-keloid-like-lesions-premature-aging-syndrome (retrieved 2026-05-03)

Canonical URL: https://4ort.xyz/entity/acroosteolysis-keloid-like-lesions-premature-aging-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. 10d ago · JhealdBatch bot · 2026-07-03 view diff on Wikidata ↗
    Mondo id → MONDO_0011150
    Genetic association → PDGFRB
    Orphanet id → 363665
    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"
Live feed via Wikidata EventStreams. New edits appear within minutes of being made on Wikidata.