CAMOS syndrome

MedicalCondition developmental_defect_during_embryogenesis Q55346076

Press Enter · cited answer in seconds

CAMOS syndrome

Summary

CAMOS syndrome is a developmental defect during embryogenesis^[1].

Key Facts

CAMOS syndrome's instance of is recorded as developmental defect during embryogenesis^[2].
CAMOS syndrome's instance of is recorded as class of disease^[3].
CAMOS syndrome is a type of autosomal recessive congenital cerebellar ataxia^[4].
CAMOS syndrome is a type of syndromic hereditary optic neuropathy^[5].
CAMOS syndrome's genetic association is recorded as WDR73^[6].
CAMOS syndrome's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_83472^[7].

⭐ Popularity Graph

0/100 long tail

Quick Facts

Instance of class of disease

Subclass of autosomal recessive congenital cerebellar ataxia, syndromic hereditary optic neuropathy, developmental defect during embryogenesis

Properties

Exact match www.orpha.net

Genetic association WDR73

External References (6)

Gard rare disease id 9977

Icd-10-cm G11.1

Mondo id MONDO_0019374

Omim id 606937

Orphanet id 83472

Umls cui C1847114, C4511633

References

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

Direct Wikidata claims

[2] ↑ CAMOS syndrome — instance of (P31): developmental defect during embryogenesis. Monarch Disease Ontology release 2018-06-29. Retrieved 2018-07-28. wikidata.org.
[3] ↑ CAMOS syndrome — instance of (P31): class of disease. wikidata.org.
[4] ↑ CAMOS syndrome — subclass of (P279): autosomal recessive congenital cerebellar ataxia. Monarch Disease Ontology release 2018-06-29. Retrieved 2018-07-03. wikidata.org.
[5] ↑ CAMOS syndrome — subclass of (P279): syndromic hereditary optic neuropathy. Monarch Disease Ontology release 2018-06-29. Retrieved 2018-07-28. wikidata.org.
[6] ↑ CAMOS syndrome — genetic association (P2293): WDR73. Open Targets Platform. Retrieved 2023-08-24. platform.opentargets.org. Provenance: wikidata.org.
[7] ↑ CAMOS syndrome — exact match (P2888): http://www.orpha.net/ORDO/Orphanet_83472. wikidata.org.

Class ancestry

[1] ↑ CAMOS syndrome is an instance of developmental defect during embryogenesis (Q55788864) [P31, primary]. 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). CAMOS syndrome. Retrieved May 3, 2026, from https://4ort.xyz/entity/camos-syndrome

MLA “CAMOS syndrome.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/camos-syndrome.

BibTeX

@misc{4ortxyz_camos-syndrome_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{CAMOS syndrome}}, year = {2026}, url = {https://4ort.xyz/entity/camos-syndrome}, note = {Accessed: 2026-05-03}}

LLM prompt

According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): CAMOS syndrome — https://4ort.xyz/entity/camos-syndrome (retrieved 2026-05-03)

Canonical URL: https://4ort.xyz/entity/camos-syndrome · Last refreshed: May 3, 2026

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.

4w ago · JhealdBatch bot · 2026-07-03 view diff on Wikidata ↗

Mondo id → MONDO_0019374

Genetic association → WDR73

Gard rare disease id → 9977

Orphanet id → 83472

+ 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.