neurofibromatoses

human diseases
MedicalCondition designated_intractable_rare_disease Q847605
neurofibromatoses
Haymanj · Public Domain · Wikimedia
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neurofibromatoses

Summary

neurofibromatoses is a designated intractable/rare disease[1]. neurofibromatoses draws 3,751 Wikipedia views per month (designated_intractable_rare_disease category, ranking #31 of 201).[2]

Key Facts

  • neurofibromatoses's instance of is recorded as designated intractable/rare disease[3].
  • neurofibromatoses's instance of is recorded as rare disease[4].
  • neurofibromatoses's instance of is recorded as class of disease[5].
  • neurofibromatoses's instance of is recorded as symptom or sign[6].
  • neurofibromatoses is a type of autosomal dominant disease[7].
  • neurofibromatoses is a type of peripheral nervous system neoplasm[8].
  • neurofibromatoses is a type of overgrowth syndrome[9].
  • neurofibromatoses is a type of disease[10].
  • neurofibromatoses's Commons category is recorded as Neurofibromatosis[11].
  • neurofibromatoses's ICPC 2 ID is recorded as A90[12].
  • neurofibromatoses's external data available at URL is recorded as http://www.nanbyou.or.jp/entry/5361[13].
  • neurofibromatoses's ICD-9-CM is recorded as 237.70[14].
  • neurofibromatoses's ICD-9-CM is recorded as 237.72[15].
  • neurofibromatoses's ICD-9-CM is recorded as 237.7[16].
  • neurofibromatoses's ICD-9-CM is recorded as 237.71[17].
  • neurofibromatoses's NCI Thesaurus ID is recorded as C6727[18].
  • neurofibromatoses's NCI Thesaurus ID is recorded as C3274[19].
  • neurofibromatoses's NCI Thesaurus ID is recorded as C3273[20].
  • neurofibromatoses's health specialty is recorded as medical genetics[21].
  • neurofibromatoses's health specialty is recorded as neurology[22].
  • neurofibromatoses's genetic association is recorded as NF1[23].
  • neurofibromatoses's genetic association is recorded as NF2[24].
  • neurofibromatoses's exact match is recorded as http://purl.obolibrary.org/obo/DOID_8712[25].
  • neurofibromatoses's exact match is recorded as http://identifiers.org/doid/DOID:8712[26].
  • neurofibromatoses's exact match is recorded as http://purl.obolibrary.org/obo/HP_0001067[27].

Why It Matters

neurofibromatoses draws 3,751 Wikipedia views per month (designated_intractable_rare_disease category, ranking #31 of 201).[2] neurofibromatoses has Wikipedia articles in 25 language editions, a strong signal of global cultural recognition.[28] neurofibromatoses 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] . ddrare.nibiohn.go.jp. Retrieved . ddrare.nibiohn.go.jp. Provenance: wikidata.org.
  2. [4] . wikidata.org.
  3. [5] . wikidata.org.
  4. [6] . wikidata.org.
  5. [7] . Disease Ontology. Retrieved . wikidata.org.
  6. [8] . wikidata.org.
  7. [9] . wikidata.org.
  8. [10] . wikidata.org.
  9. [11] . wikidata.org.
  10. [12] . wikidata.org.
  11. [13] . ddrare.nibiohn.go.jp. Retrieved . ddrare.nibiohn.go.jp. Provenance: wikidata.org.
  12. [14] . Disease Ontology. Retrieved . wikidata.org.
  13. [15] . Disease Ontology. Retrieved . wikidata.org.
  14. [16] . Disease Ontology. Retrieved . wikidata.org.
  15. [17] . Disease Ontology. Retrieved . wikidata.org.
  16. [18] . Disease Ontology. Retrieved . wikidata.org.
  17. [19] . Disease Ontology. Retrieved . wikidata.org.
  18. [20] . Disease Ontology. Retrieved . wikidata.org.
  19. [21] . wikidata.org.
  20. [22] . Klinická neurologie část speciální. wikidata.org.
  21. [23] . A clinical variant of neurofibromatosis type 1: familial spinal neurofibromatosis with a frameshift mutation in the NF1 gene. Retrieved . platform.opentargets.org. Provenance: wikidata.org.
  22. [24] . Alteration in a new gene encoding a putative membrane-organizing protein causes neuro-fibromatosis type 2. wikidata.org.
  23. [25] . Disease Ontology. Retrieved . wikidata.org.
  24. [26] . Identifiers.org. Retrieved . ebi.ac.uk. Provenance: wikidata.org.
  25. [27] . Human Phenotype Ontology release 2018-03-08. 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). neurofibromatoses. Retrieved May 3, 2026, from https://4ort.xyz/entity/neurofibromatoses
MLA “neurofibromatoses.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/neurofibromatoses.
BibTeX @misc{4ortxyz_neurofibromatoses_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{neurofibromatoses}}, year = {2026}, url = {https://4ort.xyz/entity/neurofibromatoses}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): neurofibromatoses — https://4ort.xyz/entity/neurofibromatoses (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. 12d ago · Twofivesixbot bot · 2026-05-20 view diff on Wikidata ↗
    On focus list of wikimedia project WikiProject Medicine
    Instance of
    Subclass of autosomal dominant disease, peripheral nervous system neoplasm, overgrowth syndrome +1
    Instance of designated intractable/rare disease, rare disease, class of disease +1
    + 5 other properties edited (see Wikidata diff for full list)
    "/* wbsetclaim-update-qualifiers:1||1|9 */ [[Property:P2347]]: 6082, mv to monolingual text names on YSO statements"
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