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Lujan–Fryns syndrome

rare genetic condition in humans
MedicalCondition rare_disease Q640836
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Lujan–Fryns syndrome

Summary

Lujan–Fryns syndrome is a rare disease[1]. It draws 64 Wikipedia views per month (rare_disease category, ranking #185 of 627).[2]

Key Facts

  • Lujan–Fryns syndrome's image is recorded as Lujan.jpg[3].
  • Lujan–Fryns syndrome's instance of is recorded as rare disease[4].
  • Lujan–Fryns syndrome's instance of is recorded as disease[5].
  • Lujan–Fryns syndrome's subclass of is recorded as X-linked intellectual disability[6].
  • Lujan–Fryns syndrome's Commons category is recorded as Lujan–Fryns syndrome[7].
  • Lujan–Fryns syndrome's MeSH descriptor ID is recorded as C537724[8].
  • Lujan–Fryns syndrome's OMIM ID is recorded as 309520[9].
  • Lujan–Fryns syndrome's ICD-9 ID is recorded as 317[10].
  • Lujan–Fryns syndrome's ICD-10 ID is recorded as F70.1[11].
  • Lujan–Fryns syndrome's DiseasesDB is recorded as 32654[12].
  • Lujan–Fryns syndrome's KEGG ID is recorded as H00889[13].
  • Lujan–Fryns syndrome's GeneReviews ID is recorded as NBK1676[14].
  • Lujan–Fryns syndrome's health specialty is recorded as psychiatry[15].
  • Lujan–Fryns syndrome's genetic association is recorded as MED12[16].
  • Lujan–Fryns syndrome's UMLS CUI is recorded as C0796022[17].
  • Lujan–Fryns syndrome's GARD rare disease ID is recorded as 3307[18].
  • Lujan–Fryns syndrome's Mondo ID is recorded as MONDO_0010655[19].
  • Lujan–Fryns syndrome's Microsoft Academic ID is recorded as 2781040184[20].
  • Lujan–Fryns syndrome's WikiProjectMed ID is recorded as Lujan–Fryns syndrome[21].
  • Lujan–Fryns syndrome's UniProt disease ID is recorded as DI-01917[22].

Why It Matters

Lujan–Fryns syndrome draws 64 Wikipedia views per month (rare_disease category, ranking #185 of 627).[2] It has Wikipedia articles in 9 language editions, a strong signal of global cultural recognition.[23]

Related Entities

disease psychiatry

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] ↑ . A form of X-linked mental retardation with marfanoid habitus. wikidata.org.
  4. [6] ↑ . wikidata.org.
  5. [7] ↑ . wikidata.org.
  6. [8] ↑ . wikidata.org.
  7. [9] ↑ . wikidata.org.
  8. [10] ↑ . wikidata.org.
  9. [11] ↑ . wikidata.org.
  10. [12] ↑ . wikidata.org.
  11. [13] ↑ . wikidata.org.
  12. [14] ↑ . wikidata.org.
  13. [15] ↑ . wikidata.org.
  14. [16] ↑ . The original Lujan syndrome family has a novel missense mutation (p.N1007S) in the MED12 gene. wikidata.org.
  15. [17] ↑ . wikidata.org.
  16. [18] ↑ . wikidata.org.
  17. [19] ↑ . wikidata.org.
  18. [20] ↑ . wikidata.org.
  19. [21] ↑ . wikidata.org.
  20. [22] ↑ . wikidata.org.

Class ancestry

  1. [1] ↑ . Wikidata. wikidata.org.

Aggregate / graph-position facts

  1. [2] ↑ . Wikimedia Foundation. dumps.wikimedia.org.
  2. [23] ↑ . Wikidata sitelinks. 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). Lujan–Fryns syndrome. Retrieved May 3, 2026, from https://4ort.xyz/entity/lujan-fryns-syndrome
MLA “Lujan–Fryns syndrome.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/lujan-fryns-syndrome.
BibTeX @misc{4ortxyz_lujan-fryns-syndrome_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{Lujan–Fryns syndrome}}, year = {2026}, url = {https://4ort.xyz/entity/lujan-fryns-syndrome}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): Lujan–Fryns syndrome — https://4ort.xyz/entity/lujan-fryns-syndrome (retrieved 2026-05-03)

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