von Hippel-Lindau disease

a rare genetic disorder characterized by visceral cysts and benign tumors in multiple organ systems with potential for subsequent malignant change.
MedicalCondition rare_disease Q741315
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Summary

von Hippel-Lindau disease is a rare disease[1]. It ranks in the top 0.96% of rare_disease entities by monthly Wikipedia readership (7,948 views/month, #6 of 627).[2]

Key Facts

  • von Hippel-Lindau disease's instance of is recorded as rare disease[3].
  • von Hippel-Lindau disease's instance of is recorded as class of disease[4].
  • Arvid Lindau is named after von Hippel-Lindau disease[5].
  • von Hippel-Lindau disease is a type of hemangioblastoma[6].
  • von Hippel-Lindau disease is a type of multiple polyglandular tumor[7].
  • von Hippel-Lindau disease is a type of syndromic developmental defect of the eye[8].
  • von Hippel-Lindau disease is a type of inherited nervous system cancer-predisposing syndrome[9].
  • von Hippel-Lindau disease is a type of genetic central nervous system and retinal vascular disease[10].
  • von Hippel-Lindau disease is a type of inherited renal tumor[11].
  • von Hippel-Lindau disease is a type of hereditary eye tumor[12].
  • von Hippel-Lindau disease is a type of central nervous system and retinal vascular disease[13].
  • von Hippel-Lindau disease is a type of catecholamine-producing tumor[14].
  • von Hippel-Lindau disease is a type of familial cystic renal disease[15].
  • von Hippel-Lindau disease is a type of malformation syndrome with hamartosis[16].
  • von Hippel-Lindau disease is a type of syndromic glaucoma[17].
  • von Hippel-Lindau disease is a type of developmental defect during embryogenesis[18].
  • von Hippel-Lindau disease is a type of head and neck disease[19].
  • von Hippel-Lindau disease's Commons category is recorded as Von Hippel-Lindau disease[20].
  • von Hippel-Lindau disease's described by source is recorded as The Unified Medical Dictionary (Librairie du Liban, 2009)[21].
  • von Hippel-Lindau disease's ICD-9-CM is recorded as 759.6[22].
  • von Hippel-Lindau disease's NCI Thesaurus ID is recorded as C3105[23].
  • von Hippel-Lindau disease's health specialty is recorded as medical genetics[24].
  • von Hippel-Lindau disease's health specialty is recorded as neurology[25].
  • von Hippel-Lindau disease's genetic association is recorded as VHL[26].
  • von Hippel-Lindau disease's exact match is recorded as http://purl.obolibrary.org/obo/DOID_14175[27].

Why It Matters

von Hippel-Lindau disease ranks in the top 0.96% of rare_disease entities by monthly Wikipedia readership (7,948 views/month, #6 of 627).[2] It has Wikipedia articles in 18 language editions, a strong signal of global cultural recognition.[28] It is known by 40 alternative names across languages and contexts.[29]

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] ↑ . wikidata.org.
  4. [6] ↑ . Disease Ontology. Retrieved . 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] ↑ . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  12. [14] ↑ . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  13. [15] ↑ . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  14. [16] ↑ . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  15. [17] ↑ . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  16. [18] ↑ . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  17. [19] ↑ . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  18. [20] ↑ . wikidata.org.
  19. [21] ↑ . wikidata.org.
  20. [22] ↑ . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  21. [23] ↑ . Disease Ontology. Retrieved . wikidata.org.
  22. [24] ↑ . wikidata.org.
  23. [25] ↑ . Klinická neurologie část speciální. wikidata.org.
  24. [26] ↑ . UniProt. Retrieved . search.clinicalgenome.org. Provenance: wikidata.org.
  25. [27] ↑ . Disease Ontology. Retrieved . wikidata.org.

Class ancestry

  1. [1] ↑ . Wikidata. wikidata.org.

Aggregate / graph-position facts

  1. [2] ↑ . Wikimedia Foundation. dumps.wikimedia.org.
  2. [28] ↑ . Wikidata sitelinks. wikidata.org.
  3. [29] ↑ . 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). von Hippel-Lindau disease. Retrieved October 20, 2026, from https://4ort.xyz/entity/von-hippel-lindau-disease
MLA “von Hippel-Lindau disease.” 4ort.xyz Knowledge Graph, 4ort.xyz, 20 Oct. 2026, https://4ort.xyz/entity/von-hippel-lindau-disease.
BibTeX @misc{4ortxyz_von-hippel-lindau-disease_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{von Hippel-Lindau disease}}, year = {2026}, url = {https://4ort.xyz/entity/von-hippel-lindau-disease}, note = {Accessed: 2026-10-20}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): von Hippel-Lindau disease — https://4ort.xyz/entity/von-hippel-lindau-disease (retrieved 2026-10-20)

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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. 23d ago · فيصل · 2026-09-27 view diff on Wikidata ↗
    Wikipedia languages → ['ar', 'bs', 'ca', 'commons', 'da', 'de', 'el', 'en', 'es', 'fa', 'fi', 'fr', 'h
    Described by source → The Unified Medical Dictionary (Librairie du Liban, 2009)
    Gnd id → 4167688-9
    Claims rich → —
    "/* wbsetclaim-create:2||1 */ Described by source: The Unified Medical Dictionary (Librairie du Liban, 2009)"
  2. 15w ago · JhealdBatch bot · 2026-07-03 view diff on Wikidata ↗
    Subclass of → hemangioblastoma, multiple polyglandular tumor, syndromic developmental defect of the eye +11
    Instance of → rare disease, class of disease
    "/* wbeditentity-update:0| */ QuickStatements 3.0 [[:toollabs:qs-dev/batch/39742|batch #39742]]: subclass of disease, not instance"
  3. 15w ago · JhealdBatch bot · 2026-07-03 view diff on Wikidata ↗
    Subclass of → hemangioblastoma, multiple polyglandular tumor, syndromic developmental defect of the eye +11
    "/* wbeditentity-update:0| */ QuickStatements 3.0 [[:toollabs:qs-dev/batch/39732|batch #39732]]: rm redundant subclass"
  4. 21w ago · Comfyquiettree · 2026-05-24 view diff on Wikidata ↗
    Wikiskripta article id → 54771
    "/* wbsetclaim-create:1||1 */ Wikiskripta article id: 54771, Matched to [[:toollabs:mix-n-match/#/entry/78317137|Syndrom von Hippel-Lindau (#78317137)]] in [[:toollabs:mix-n-match/#/catalog/2686|WikiSk"
  5. 21w ago · Twofivesixbot bot · 2026-05-20 view diff on Wikidata ↗
    On focus list of wikimedia project → WikiProject Medicine
    Named after → Arvid Lindau
    Instance of → —
    Subclass of → hemangioblastoma, multiple polyglandular tumor, syndromic developmental defect of the eye +11
    + 7 other properties edited (see Wikidata diff for full list)
    "/* wbsetclaim-update-qualifiers:1||1|11 */ Yso id: 21521, mv to monolingual text names on YSO statements"
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