Werner syndrome

Lethal autosomal recessive disorder
MedicalCondition designated_intractable_rare_disease Q1154619
Press Enter · cited answer in seconds

Werner syndrome

Summary

Werner syndrome is a designated intractable/rare disease[1]. It draws 3,688 Wikipedia views per month (designated_intractable_rare_disease category, ranking #78 of 201).[2]

Key Facts

  • Werner syndrome's instance of is recorded as designated intractable/rare disease[3].
  • Werner syndrome's instance of is recorded as developmental defect during embryogenesis[4].
  • Werner syndrome's instance of is recorded as rare disease[5].
  • Werner syndrome's instance of is recorded as class of disease[6].
  • Werner syndrome is a type of autosomal recessive disease[7].
  • Werner syndrome is a type of progeroid syndrome[8].
  • Werner syndrome is a type of ectodermal malformation syndrome associated with ocular features[9].
  • Werner syndrome is a type of hereditary poikiloderma[10].
  • Werner syndrome is a type of malformation syndrome with skin/mucosae involvement[11].
  • Werner syndrome is a type of polymalformative genetic syndrome with increased risk of developing cancer[12].
  • Werner syndrome is a type of syndrome[13].
  • Werner syndrome is a type of disease[14].
  • Werner syndrome's external data available at URL is recorded as http://www.nanbyou.or.jp/entry/5320[15].
  • Werner syndrome's ICD-9-CM is recorded as 259.8[16].
  • Werner syndrome's NCI Thesaurus ID is recorded as C3447[17].
  • Werner syndrome's different from is recorded as hypoplastic tibiae-postaxial polydactyly syndrome[18].
  • Werner syndrome's health specialty is recorded as endocrinology[19].
  • Werner syndrome's genetic association is recorded as WRN[20].
  • Werner syndrome's exact match is recorded as http://purl.obolibrary.org/obo/DOID_5688[21].
  • Werner syndrome's exact match is recorded as http://identifiers.org/doid/DOID:5688[22].
  • Werner syndrome's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_902[23].
  • Werner syndrome's on focus list of Wikimedia project is recorded as WikiProject Medicine[24].

Why It Matters

Werner syndrome draws 3,688 Wikipedia views per month (designated_intractable_rare_disease category, ranking #78 of 201).[2] It has Wikipedia articles in 16 language editions, a strong signal of global cultural recognition.[25] It is known by 18 alternative names across languages and contexts.[26]

References

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

Direct Wikidata claims

  1. [3] . ddrare.nibiohn.go.jp. Retrieved . ddrare.nibiohn.go.jp. Provenance: wikidata.org.
  2. [4] . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  3. [5] . wikidata.org.
  4. [6] . wikidata.org.
  5. [7] . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  6. [8] . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  7. [9] . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  8. [10] . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  9. [11] . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  10. [12] . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  11. [13] . Disease Ontology. Retrieved . wikidata.org.
  12. [14] . wikidata.org.
  13. [15] . ddrare.nibiohn.go.jp. Retrieved . ddrare.nibiohn.go.jp. Provenance: wikidata.org.
  14. [16] . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  15. [17] . Disease Ontology. Retrieved . wikidata.org.
  16. [18] . wikidata.org.
  17. [19] . wikidata.org.
  18. [20] . Q905695. Retrieved . search.clinicalgenome.org. Provenance: wikidata.org.
  19. [21] . Disease Ontology. Retrieved . wikidata.org.
  20. [22] . Identifiers.org. registry.identifiers.org. Provenance: wikidata.org.
  21. [23] . wikidata.org.
  22. [24] . wikidata.org.

Class ancestry

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

Aggregate / graph-position facts

  1. [2] . Wikimedia Foundation. dumps.wikimedia.org.
  2. [25] . Wikidata sitelinks. wikidata.org.
  3. [26] . 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). Werner syndrome. Retrieved May 3, 2026, from https://4ort.xyz/entity/werner-syndrome
MLA “Werner syndrome.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/werner-syndrome.
BibTeX @misc{4ortxyz_werner-syndrome_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{Werner syndrome}}, year = {2026}, url = {https://4ort.xyz/entity/werner-syndrome}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): Werner syndrome — https://4ort.xyz/entity/werner-syndrome (retrieved 2026-05-03)

Canonical URL: https://4ort.xyz/entity/werner-syndrome · 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. 5d ago · Twofivesixbot bot · 2026-05-27 view diff on Wikidata ↗
    Health specialty endocrinology
    Instance of designated intractable/rare disease, developmental defect during embryogenesis, rare disease +1
    Subclass of
    Aliases
    + 5 other properties edited (see Wikidata diff for full list)
    "/* wbsetclaim-update-qualifiers:1||1|2 */ [[Property:P8189]]: 987007553632705171, mv to monolingual text names on J9U statements"
Live feed via Wikidata EventStreams. New edits appear within minutes of being made on Wikidata.