mosaic trisomy 22

MedicalCondition developmental_defect_during_embryogenesis Q55788938

Press Enter · cited answer in seconds

mosaic trisomy 22

Summary

mosaic trisomy 22 is a developmental defect during embryogenesis^[1].

Key Facts

mosaic trisomy 22's instance of is recorded as developmental defect during embryogenesis^[2].
mosaic trisomy 22's instance of is recorded as class of disease^[3].
mosaic trisomy 22 is a type of total autosomal trisomy^[4].
mosaic trisomy 22 is a type of trisomy 22^[5].
mosaic trisomy 22's different from is recorded as trisomy 22^[6].
mosaic trisomy 22's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_96068^[7].

⭐ Popularity Graph

0/100 long tail

Quick Facts

Instance of class of disease

Subclass of total autosomal trisomy, trisomy 22, developmental defect during embryogenesis

Properties

Different from trisomy 22

Exact match www.orpha.net

External References (6)

Gard rare disease id 6085

Icd-10-cm Q92.1

Mesh descriptor id C536796

Mondo id MONDO_0019869

Orphanet id 96068

Umls cui C2931326, C2931327

References

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

Direct Wikidata claims

[2] ↑ mosaic trisomy 22 — instance of (P31): developmental defect during embryogenesis. Monarch Disease Ontology release 2018-06-29. Retrieved 2018-07-28. wikidata.org.
[3] ↑ mosaic trisomy 22 — instance of (P31): class of disease. wikidata.org.
[4] ↑ mosaic trisomy 22 — subclass of (P279): total autosomal trisomy. Monarch Disease Ontology release 2018-06-29. Retrieved 2018-07-28. wikidata.org.
[5] ↑ mosaic trisomy 22 — subclass of (P279): trisomy 22. wikidata.org.
[6] ↑ mosaic trisomy 22 — different from (P1889): trisomy 22. wikidata.org.
[7] ↑ mosaic trisomy 22 — exact match (P2888): http://www.orpha.net/ORDO/Orphanet_96068. wikidata.org.

Class ancestry

[1] ↑ mosaic trisomy 22 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). mosaic trisomy 22. Retrieved May 3, 2026, from https://4ort.xyz/entity/mosaic-trisomy-22

MLA “mosaic trisomy 22.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/mosaic-trisomy-22.

BibTeX

@misc{4ortxyz_mosaic-trisomy-22_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{mosaic trisomy 22}}, year = {2026}, url = {https://4ort.xyz/entity/mosaic-trisomy-22}, note = {Accessed: 2026-05-03}}

LLM prompt

According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): mosaic trisomy 22 — https://4ort.xyz/entity/mosaic-trisomy-22 (retrieved 2026-05-03)

Canonical URL: https://4ort.xyz/entity/mosaic-trisomy-22 · 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.

19d ago · JhealdBatch bot · 2026-07-03 view diff on Wikidata ↗

Mondo id → MONDO_0019869

Gard rare disease id → 6085

Orphanet id → 96068

Different from → trisomy 22

+ 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.