multiple epiphyseal dysplasia

osteochondrodysplasia that has material basis in defective cartilage mineralization into bone which results in irregular ossification centers of the located in hip or located in knee. The disease has symptom fatigue, has symptom joint pain
MedicalCondition genetic_disease Q1452604
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multiple epiphyseal dysplasia

Summary

multiple epiphyseal dysplasia is a genetic disease[1]. It has Wikipedia articles in 8 language editions, a strong signal of global cultural recognition.[2]

Key Facts

  • multiple epiphyseal dysplasia's instance of is recorded as genetic disease[3].
  • multiple epiphyseal dysplasia's instance of is recorded as developmental defect during embryogenesis[4].
  • multiple epiphyseal dysplasia's instance of is recorded as rare disease[5].
  • multiple epiphyseal dysplasia's instance of is recorded as class of disease[6].
  • multiple epiphyseal dysplasia is a type of osteochondrodysplasia[7].
  • multiple epiphyseal dysplasia's Commons category is recorded as Multiple epiphyseal dysplasia[8].
  • multiple epiphyseal dysplasia's symptoms and signs is recorded as arthralgia[9].
  • multiple epiphyseal dysplasia's ICD-9-CM is recorded as 756.56[10].
  • multiple epiphyseal dysplasia's health specialty is recorded as medical genetics[11].
  • multiple epiphyseal dysplasia's genetic association is recorded as COL9A2[12].
  • multiple epiphyseal dysplasia's genetic association is recorded as COL9A3[13].
  • multiple epiphyseal dysplasia's genetic association is recorded as COL9A1[14].
  • multiple epiphyseal dysplasia's exact match is recorded as http://purl.obolibrary.org/obo/DOID_12721[15].
  • multiple epiphyseal dysplasia's exact match is recorded as http://identifiers.org/doid/DOID:12721[16].
  • multiple epiphyseal dysplasia's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_166002[17].
  • multiple epiphyseal dysplasia's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_251[18].
  • multiple epiphyseal dysplasia's on focus list of Wikimedia project is recorded as WikiProject Medicine[19].

Why It Matters

multiple epiphyseal dysplasia has Wikipedia articles in 8 language editions, a strong signal of global cultural recognition.[2] It is known by 6 alternative names across languages and contexts.[20]

References

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

Direct Wikidata claims

  1. [3] . wikidata.org.
  2. [4] . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  3. [5] . wikidata.org.
  4. [6] . wikidata.org.
  5. [7] . Disease Ontology. Retrieved . wikidata.org.
  6. [8] . wikidata.org.
  7. [9] . Disease Ontology. Retrieved . wikidata.org.
  8. [10] . Disease Ontology. Retrieved . wikidata.org.
  9. [11] . wikidata.org.
  10. [12] . A mutation in the gene encoding the alpha 2 chain of the fibril-associated collagen IX, COL9A2, causes multiple epiphyseal dysplasia (EDM2). wikidata.org.
  11. [13] . COL9A3: A third locus for multiple epiphyseal dysplasia. wikidata.org.
  12. [14] . A mutation in COL9A1 causes multiple epiphyseal dysplasia: further evidence for locus heterogeneity. wikidata.org.
  13. [15] . Disease Ontology. Retrieved . wikidata.org.
  14. [16] . Identifiers.org. registry.identifiers.org. Provenance: wikidata.org.
  15. [17] . wikidata.org.
  16. [18] . wikidata.org.
  17. [19] . wikidata.org.

Class ancestry

  1. [1] . Wikidata. wikidata.org.

Aggregate / graph-position facts

  1. [2] . Wikidata sitelinks. wikidata.org.
  2. [20] . Wikidata aliases. 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). multiple epiphyseal dysplasia. Retrieved May 3, 2026, from https://4ort.xyz/entity/multiple-epiphyseal-dysplasia
MLA “multiple epiphyseal dysplasia.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/multiple-epiphyseal-dysplasia.
BibTeX @misc{4ortxyz_multiple-epiphyseal-dysplasia_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{multiple epiphyseal dysplasia}}, year = {2026}, url = {https://4ort.xyz/entity/multiple-epiphyseal-dysplasia}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): multiple epiphyseal dysplasia — https://4ort.xyz/entity/multiple-epiphyseal-dysplasia (retrieved 2026-05-03)

Canonical URL: https://4ort.xyz/entity/multiple-epiphyseal-dysplasia · 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. 5w ago · JhealdBatch bot · 2026-07-03 view diff on Wikidata ↗
    Health specialty medical genetics
    Genetic association COL9A2, COL9A3, COL9A1
    Subclass of
    Instance of genetic disease, developmental defect during embryogenesis, rare disease +1
    + 5 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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