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Opsismodysplasia

Opsismodysplasia is a skeletal dysplasia characterized by congenital dwarfism and facial dysmorphism
MedicalCondition developmental_defect_during_embryogenesis Q7098730
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Opsismodysplasia

Summary

Opsismodysplasia is a developmental defect during embryogenesis[1]. Opsismodysplasia draws 149 Wikipedia views per month (developmental_defect_during_embryogenesis category, ranking #135 of 308).[2]

Key Facts

  • Opsismodysplasia's instance of is recorded as developmental defect during embryogenesis[3].
  • Opsismodysplasia's instance of is recorded as rare disease[4].
  • Opsismodysplasia's instance of is recorded as class of disease[5].
  • Opsismodysplasia is a type of osteochondrodysplasia[6].
  • Opsismodysplasia is a type of Spondylodysplastic dysplasia[7].
  • Opsismodysplasia's health specialty is recorded as medical genetics[8].
  • Opsismodysplasia's genetic association is recorded as INPPL1[9].
  • Opsismodysplasia's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_2746[10].

Why It Matters

Opsismodysplasia draws 149 Wikipedia views per month (developmental_defect_during_embryogenesis category, ranking #135 of 308).[2] Opsismodysplasia is known by 4 alternative names across languages and contexts.[11]

References

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

Direct Wikidata claims

  1. [3] ↑ . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  2. [4] ↑ . wikidata.org.
  3. [5] ↑ . wikidata.org.
  4. [6] ↑ . wikidata.org.
  5. [7] ↑ . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  6. [8] ↑ . wikidata.org.
  7. [9] ↑ . Q905695. Retrieved . platform.opentargets.org. Provenance: wikidata.org.
  8. [10] ↑ . wikidata.org.

Class ancestry

  1. [1] ↑ . Wikidata. wikidata.org.

Aggregate / graph-position facts

  1. [2] ↑ . Wikimedia Foundation. dumps.wikimedia.org.
  2. [11] ↑ . 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). Opsismodysplasia. Retrieved May 3, 2026, from https://4ort.xyz/entity/opsismodysplasia
MLA “Opsismodysplasia.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/opsismodysplasia.
BibTeX @misc{4ortxyz_opsismodysplasia_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{Opsismodysplasia}}, year = {2026}, url = {https://4ort.xyz/entity/opsismodysplasia}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): Opsismodysplasia — https://4ort.xyz/entity/opsismodysplasia (retrieved 2026-05-03)

Canonical URL: https://4ort.xyz/entity/opsismodysplasia · 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. 10w ago · JhealdBatch bot · 2026-07-03 view diff on Wikidata ↗
    Mondo id → MONDO_0009785
    Orphanet id → 2746
    Imported from → —
    Mesh descriptor id → C537122
    + 17 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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