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Fraser syndrome

autosomal recessive congenital disorder
Class type of: cryptophthalmos, autosomal recessive disease, syndromic genetic deafness Q1425572

Facts

11 properties
Instance of
class of disease
Subclass of
cryptophthalmos, autosomal recessive disease, syndromic genetic deafness, syndromic renal or urinary tract malformation, syndromic developmental defect of the eye, syndromic anorectal malformation, multiple congenital anomalies/dysmorphic syndrome without intellectual disability, syndrome, disorder of sex development, 46,XY, developmental defect during embryogenesis, head and neck disease[7][8][9][10][11][12][13]
Age of onset
congenital onset, neonatal onset[20][21]
Different from
Frasier syndrome[15]
Genetic association
FRAS1, FREM2, GRIP1[17][18][19]
Has phenotype
seizure, Subglottic stenosis[23][24]
Health specialty
medical genetics[16]
NCI Thesaurus ID
C118436[14]
Named after
George R. Fraser[6]
On focus list of Wikimedia project
WikiProject Medicine[22]
P14914
D02052[25]
🏷️ Also known as
en FRASER SYNDROME en Meyer-Schwickerath's syndrome en Ulrich-Feichtiger syndrome en Cryptophthalmos-Syndactyly Syndrome en Cryptophthalmos syndrome en cryptophthalmos with other malformations en Cyclopism en Fraser-Francois syndrome en Fraser syndrome ar فرسر سيندروم ar متلازمة فرسر de Fraser-Syndrom es síndrome de Fraser fi Fraserin oireyhtymä fi Fraserin syndrooma fr syndrome de Fraser ja フレイザー症候群 pl Zespół Frasera pl Zespół Ullricha-Feichtigera ru Синдром Фрейзера
🔖 Identifiers · 25
Image (Wikimedia Commons)
Fraser syndrome.gif ↗
DeCS ID
53969
Disease Ontology ID
DOID:0090001
DiseasesDB
32241
Exact match
purl.obolibrary.org, identifiers.org, www.orpha.net
Freebase ID
/m/07wtzn
GARD rare disease ID
6465
Genetics Home Reference Conditions ID
fraser-syndrome
Homosaurus ID (V3)
homoit0002839
Homosaurus ID (V4)
homoit0002839
ICD-10-CM
Q87.0
ICD-11 ID (Foundation)
968262849
Show all 25 identifiers +13
ICD-11 ID (MMS)
LD2H.0
JSTOR topic ID (archived)
fraser-syndrome
KEGG ID
H00687
MeSH descriptor ID
D058497
MeSH tree code
C05.116.099.370.894.819.428, C05.660.585.800.428, C05.660.906.819.428, C11.250.390, C16.131.077.371, C16.131.384.442, C16.131.621.585.800.428, C16.131.621.906.819.428, C16.131.939.410, C12.050.351.875.397, C12.200.706.410, C12.800.410
Microsoft Academic ID (discontinued)
2779064689, 2908634241
Mondo ID
MONDO_0009046
OMIM ID
219000
Orphanet ID
2052
SNOMED CT ID
204102004
UMLS CUI
C0265233
Wellcome Collection concept ID
s2mfudgf
WikiProjectMed ID
Fraser syndrome

Report an error or request removal Lineage (PROV-JSON)

🔗 Connections
Genetic association 2
GRIP1, FREM2
← Genetic association 2
GRIP1, FREM2
Health specialty 1
medical genetics
On focus list of Wikimedia project 1
WikiProject Medicine
Subclass of 1
syndrome
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Summary

Fraser syndrome is a class of disease[1]. It is a type of cryptophthalmos[2], autosomal recessive disease[3], syndromic genetic deafness[4], and syndromic renal or urinary tract malformation[5].

References

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

Direct Wikidata claims

  1. [6] ↑ . wikidata.org.
  2. [2] ↑ . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  3. [3] ↑ . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  4. [4] ↑ . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  5. [5] ↑ . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  6. [7] ↑ . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  7. [8] ↑ . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  8. [9] ↑ . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  9. [10] ↑ . Disease Ontology. Retrieved . wikidata.org.
  10. [11] ↑ . orpha.net. orpha.net. Provenance: wikidata.org.
  11. [12] ↑ . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  12. [13] ↑ . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  13. [14] ↑ . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  14. [15] ↑ . wikidata.org.
  15. [16] ↑ . wikidata.org.
  16. [17] ↑ . UniProt. Retrieved . platform.opentargets.org. Provenance: wikidata.org.
  17. [18] ↑ . Open Targets Platform. Retrieved . platform.opentargets.org. Provenance: wikidata.org.
  18. [19] ↑ . Open Targets Platform. Retrieved . platform.opentargets.org. Provenance: wikidata.org.
  19. [20] ↑ . Retrieved . wikidata.org.
  20. [21] ↑ . Retrieved . wikidata.org.
  21. [22] ↑ . wikidata.org.
  22. [23] ↑ . Retrieved . wikidata.org.
  23. [24] ↑ . Retrieved . wikidata.org.
  24. [25] ↑ . wikidata.org.

Class ancestry

  1. [1] ↑ . Wikidata. 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 November 1, 2026, from https://4ort.xyz/entity/fraser-syndrome
MLA “Fraser syndrome.” 4ort.xyz Knowledge Graph, 4ort.xyz, 1 Nov. 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: 2026-11-01}}
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 2026-11-01)

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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 · ACorrêa (WMB) · 2026-10-23 view diff on Wikidata ↗
    Wikipedia languages → ['ar', 'commons', 'de', 'en', 'fi', 'pl', 'ru', 'tr']
    Age of onset → congenital onset, neonatal onset
    Has phenotype → seizure, Subglottic stenosis
    P14914 → D02052
    + 1 other property edited (see Wikidata diff for full list)
    "/* wbeditentity-update-languages-and-other-short:0||pt, pt-br */ QuickStatements 3.0 [[:toollabs:qs-dev/batch/61469|batch #61469]]: Raras.org data import"
  2. 17w ago · JhealdBatch bot · 2026-07-03 view diff on Wikidata ↗
    Subclass of → cryptophthalmos, autosomal recessive disease, syndromic genetic deafness +8
    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"
Live feed via Wikidata EventStreams. New edits appear within minutes of being made on Wikidata.