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spondyloepiphyseal dysplasia

rare human disease
MedicalCondition hereditary_disorder Q7578956
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spondyloepiphyseal dysplasia

Summary

spondyloepiphyseal dysplasia is a hereditary disorder[1].

Key Facts

  • spondyloepiphyseal dysplasia's instance of is recorded as hereditary disorder[2].
  • spondyloepiphyseal dysplasia's instance of is recorded as class of disease[3].
  • spondyloepiphyseal dysplasia is a type of osteochondrodysplasia[4].
  • spondyloepiphyseal dysplasia's Commons category is recorded as Spondyloepiphyseal dysplasia[5].

References

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

Direct Wikidata claims

  1. [2] ↑ . wikidata.org.
  2. [3] ↑ . wikidata.org.
  3. [4] ↑ . Schimke immuno-osseous dysplasia: case report and review of 25 patients. wikidata.org.
  4. [5] ↑ . 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). spondyloepiphyseal dysplasia. Retrieved May 3, 2026, from https://4ort.xyz/entity/spondyloepiphyseal-dysplasia
MLA “spondyloepiphyseal dysplasia.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/spondyloepiphyseal-dysplasia.
BibTeX @misc{4ortxyz_spondyloepiphyseal-dysplasia_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{spondyloepiphyseal dysplasia}}, year = {2026}, url = {https://4ort.xyz/entity/spondyloepiphyseal-dysplasia}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): spondyloepiphyseal dysplasia — https://4ort.xyz/entity/spondyloepiphyseal-dysplasia (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. 1d ago · JhealdBatch bot · 2026-07-03 view diff on Wikidata ↗
    Gard rare disease id → 7687
    Orphanet id → 253
    Instance of → hereditary disorder, class of disease
    Commons category → Spondyloepiphyseal dysplasia
    + 4 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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