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Stüve-Wiedemann syndrome

human disease
MedicalCondition hereditary_disorder Q9182808
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Summary

Stüve-Wiedemann syndrome is a hereditary disorder[1]. It is known by 20 alternative names across languages and contexts.[2]

Key Facts

  • Instance of: rare disease[3], osteochondrodysplasia[4], developmental defect during embryogenesis[5], class of disease[6]
  • Named after: Hans-Rudolf Wiedemann[7]
  • Subclass of: bent bone dysplasia[8]
  • Commons category: Stuve-Wiedemann syndrome[9]
  • Genetic association: LIFR[10]
  • Exact match: http://www.orpha.net/ORDO/Orphanet_3206[11]

References

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

Direct Wikidata claims

  1. [3] ↑ . wikidata.org.
  2. [4] ↑ . wikidata.org.
  3. [5] ↑ . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  4. [6] ↑ . wikidata.org.
  5. [7] ↑ . wikidata.org.
  6. [8] ↑ . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  7. [9] ↑ . wikidata.org.
  8. [10] ↑ . UniProt. Retrieved . search.clinicalgenome.org. Provenance: wikidata.org.
  9. [11] ↑ . wikidata.org.

Class ancestry

  1. [1] ↑ . Wikidata. wikidata.org.

Aggregate / graph-position facts

  1. [2] ↑ . 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). Stüve-Wiedemann syndrome. Retrieved October 18, 2026, from https://4ort.xyz/entity/st-ve-wiedemann-syndrome
MLA “Stüve-Wiedemann syndrome.” 4ort.xyz Knowledge Graph, 4ort.xyz, 18 Oct. 2026, https://4ort.xyz/entity/st-ve-wiedemann-syndrome.
BibTeX @misc{4ortxyz_st-ve-wiedemann-syndrome_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{Stüve-Wiedemann syndrome}}, year = {2026}, url = {https://4ort.xyz/entity/st-ve-wiedemann-syndrome}, note = {Accessed: 2026-10-18}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): Stüve-Wiedemann syndrome — https://4ort.xyz/entity/st-ve-wiedemann-syndrome (retrieved 2026-10-18)

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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. 15w ago · JhealdBatch bot · 2026-07-03 view diff on Wikidata ↗
    Mondo id → MONDO_0011108
    Genetic association → LIFR
    Gard rare disease id → 5045
    Orphanet id → 3206
    + 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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