Fraser syndrome

autosomal recessive congenital disorder
MedicalCondition head_and_neck_disease Q1425572
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Fraser syndrome

Summary

Fraser syndrome is a head and neck disease[1]. It has Wikipedia articles in 7 language editions, a strong signal of global cultural recognition.[2]

Key Facts

  • Fraser syndrome's instance of is recorded as head and neck disease[3].
  • Fraser syndrome's instance of is recorded as developmental defect during embryogenesis[4].
  • Fraser syndrome's instance of is recorded as class of disease[5].
  • George R. Fraser is named after Fraser syndrome[6].
  • Fraser syndrome is a type of cryptophthalmos[7].
  • Fraser syndrome is a type of autosomal recessive disease[8].
  • Fraser syndrome is a type of syndromic genetic deafness[9].
  • Fraser syndrome is a type of syndromic renal or urinary tract malformation[10].
  • Fraser syndrome is a type of syndromic developmental defect of the eye[11].
  • Fraser syndrome is a type of syndromic anorectal malformation[12].
  • Fraser syndrome is a type of multiple congenital anomalies/dysmorphic syndrome without intellectual disability[13].
  • Fraser syndrome is a type of syndrome[14].
  • Fraser syndrome is a type of disorder of sex development, 46,XY[15].
  • Fraser syndrome's Commons category is recorded as Fraser syndrome[16].
  • Fraser syndrome's NCI Thesaurus ID is recorded as C118436[17].
  • Fraser syndrome's different from is recorded as Frasier syndrome[18].
  • Fraser syndrome's health specialty is recorded as medical genetics[19].
  • Fraser syndrome's genetic association is recorded as FRAS1[20].
  • Fraser syndrome's genetic association is recorded as FREM2[21].
  • Fraser syndrome's genetic association is recorded as GRIP1[22].
  • Fraser syndrome's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0090001[23].
  • Fraser syndrome's exact match is recorded as http://identifiers.org/doid/DOID:0090001[24].
  • Fraser syndrome's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_2052[25].
  • Fraser syndrome's on focus list of Wikimedia project is recorded as WikiProject Medicine[26].

Why It Matters

Fraser syndrome has Wikipedia articles in 7 language editions, a strong signal of global cultural recognition.[2] It is known by 11 alternative names across languages and contexts.[27]

References

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

Direct Wikidata claims

  1. [3] . Monarch Disease Ontology release 2018-06-29. Retrieved . 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] . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  12. [14] . Disease Ontology. Retrieved . wikidata.org.
  13. [15] . orpha.net. orpha.net. Provenance: wikidata.org.
  14. [16] . wikidata.org.
  15. [17] . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  16. [18] . wikidata.org.
  17. [19] . wikidata.org.
  18. [20] . Q905695. Retrieved . platform.opentargets.org. Provenance: wikidata.org.
  19. [21] . Open Targets Platform. Retrieved . platform.opentargets.org. Provenance: wikidata.org.
  20. [22] . Open Targets Platform. Retrieved . platform.opentargets.org. Provenance: wikidata.org.
  21. [23] . Disease Ontology. Retrieved . wikidata.org.
  22. [24] . Identifiers.org. registry.identifiers.org. Provenance: wikidata.org.
  23. [25] . wikidata.org.
  24. [26] . wikidata.org.

Class ancestry

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

Aggregate / graph-position facts

  1. [2] . Wikidata sitelinks. wikidata.org.
  2. [27] . 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). Fraser syndrome. Retrieved May 3, 2026, from https://4ort.xyz/entity/fraser-syndrome
MLA “Fraser syndrome.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/fraser-syndrome.
BibTeX @misc{4ortxyz_fraser-syndrome_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{Fraser syndrome}}, year = {2026}, url = {https://4ort.xyz/entity/fraser-syndrome}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): Fraser syndrome — https://4ort.xyz/entity/fraser-syndrome (retrieved 2026-05-03)

Canonical URL: https://4ort.xyz/entity/fraser-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. 17d ago · JhealdBatch bot · 2026-07-03 view diff on Wikidata ↗
    Subclass of cryptophthalmos, autosomal recessive disease, syndromic genetic deafness +6
    Named after
    Health specialty medical genetics
    Genetic association FRAS1, FREM2, GRIP1
    + 7 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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