Polyostotic osteolytic dysplasia, hereditary expansile

human disease
MedicalCondition developmental_defect_during_embryogenesis Q43396517
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Polyostotic osteolytic dysplasia, hereditary expansile

Summary

Polyostotic osteolytic dysplasia, hereditary expansile is a developmental defect during embryogenesis[1].

Key Facts

  • Polyostotic osteolytic dysplasia, hereditary expansile's instance of is recorded as developmental defect during embryogenesis[2].
  • Polyostotic osteolytic dysplasia, hereditary expansile's instance of is recorded as rare disease[3].
  • Polyostotic osteolytic dysplasia, hereditary expansile's instance of is recorded as class of disease[4].
  • Polyostotic osteolytic dysplasia, hereditary expansile is a type of osteolysis[5].
  • Polyostotic osteolytic dysplasia, hereditary expansile is a type of primary osteolysis[6].
  • Polyostotic osteolytic dysplasia, hereditary expansile is a type of autosomal dominant disease[7].
  • Polyostotic osteolytic dysplasia, hereditary expansile is a type of bone remodeling disease[8].
  • Polyostotic osteolytic dysplasia, hereditary expansile's ICD-9-CM is recorded as 756.9[9].
  • Polyostotic osteolytic dysplasia, hereditary expansile's genetic association is recorded as TNFRSF11A[10].
  • Polyostotic osteolytic dysplasia, hereditary expansile's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_85195[11].
  • Polyostotic osteolytic dysplasia, hereditary expansile's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0111542[12].
  • Polyostotic osteolytic dysplasia, hereditary expansile's exact match is recorded as http://identifiers.org/doid/DOID:0111542[13].

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] . wikidata.org.
  5. [6] . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  6. [7] . Disease Ontology. Retrieved . wikidata.org.
  7. [8] . Disease Ontology. Retrieved . wikidata.org.
  8. [9] . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  9. [10] . Q905695. Retrieved . wikidata.org.
  10. [11] . wikidata.org.
  11. [12] . Disease Ontology. Retrieved . wikidata.org.
  12. [13] . Identifiers.org. registry.identifiers.org. Provenance: 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). Polyostotic osteolytic dysplasia, hereditary expansile. Retrieved May 3, 2026, from https://4ort.xyz/entity/polyostotic-osteolytic-dysplasia-hereditary-expansile
MLA “Polyostotic osteolytic dysplasia, hereditary expansile.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/polyostotic-osteolytic-dysplasia-hereditary-expansile.
BibTeX @misc{4ortxyz_polyostotic-osteolytic-dysplasia-hereditary-expansile_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{Polyostotic osteolytic dysplasia, hereditary expansile}}, year = {2026}, url = {https://4ort.xyz/entity/polyostotic-osteolytic-dysplasia-hereditary-expansile}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): Polyostotic osteolytic dysplasia, hereditary expansile — https://4ort.xyz/entity/polyostotic-osteolytic-dysplasia-hereditary-expansile (retrieved 2026-05-03)

Canonical URL: https://4ort.xyz/entity/polyostotic-osteolytic-dysplasia-hereditary-expansile · 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. 2d ago · JhealdBatch bot · 2026-07-03 view diff on Wikidata ↗
    Mondo id MONDO_0008275
    Genetic association TNFRSF11A
    Gard rare disease id 9168
    Orphanet id 85195
    + 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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