Luscan-Lumish syndrome

human disease

MedicalCondition rare_disease Q55785011

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Summary

Luscan-Lumish syndrome is a rare disease^[1].

Key Facts

Luscan-Lumish syndrome's instance of is recorded as rare disease^[2].
Luscan-Lumish syndrome's instance of is recorded as disease^[3].
Luscan-Lumish syndrome is a type of genetic disease^[4].
Luscan-Lumish syndrome is a type of Sotos syndrome^[5].
Luscan-Lumish syndrome's genetic association is recorded as SETD2^[6].

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Quick Facts

Instance of rare disease, class of disease

Subclass of genetic disease, Sotos syndrome

Properties

Genetic association SETD2

External References (5)

Kegg id H02444

Mondo id MONDO_0014791

Omim id 616831

Umls cui C4085873

Uniprot disease id DI-04661

🌐 Available in 2 languages

enLuscan–Lumish syndrome fiLuscan–Lumishin oireyhtymä

🏷️ Also known as

en LLS en Luscan-Lumish syndrome en Sotos-like syndrome fi Luscan–Lumishin oireyhtymä fr syndrome de Luscan-Lumish fr syndrome de Sotos LIKE

References

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

Direct Wikidata claims

[2] ↑ Luscan-Lumish syndrome — instance of (P31): rare disease. wikidata.org.
[3] ↑ Luscan-Lumish syndrome — instance of (P31): disease. Sporadic autism exomes reveal a highly interconnected protein network of de novo mutations. wikidata.org.
[4] ↑ Luscan-Lumish syndrome — subclass of (P279): genetic disease. Monarch Disease Ontology release 2018-06-29. Retrieved 2018-07-28. wikidata.org.
[5] ↑ Luscan-Lumish syndrome — subclass of (P279): Sotos syndrome. wikidata.org.
[6] ↑ Luscan-Lumish syndrome — genetic association (P2293): SETD2. Sporadic autism exomes reveal a highly interconnected protein network of de novo mutations. Retrieved 2023-08-24. platform.opentargets.org. Provenance: wikidata.org.

Class ancestry

[1] ↑ Luscan-Lumish syndrome is an instance of rare disease (Q929833) [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). Luscan-Lumish syndrome. Retrieved October 20, 2026, from https://4ort.xyz/entity/luscan-lumish-syndrome

MLA

“Luscan-Lumish syndrome.” 4ort.xyz Knowledge Graph, 4ort.xyz, 20 Oct. 2026, https://4ort.xyz/entity/luscan-lumish-syndrome.

BibTeX

@misc{4ortxyz_luscan-lumish-syndrome_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{Luscan-Lumish syndrome}}, year = {2026}, url = {https://4ort.xyz/entity/luscan-lumish-syndrome}, note = {Accessed: 2026-10-20}}

LLM prompt

According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): Luscan-Lumish syndrome — https://4ort.xyz/entity/luscan-lumish-syndrome (retrieved 2026-10-20)

Canonical URL: https://4ort.xyz/entity/luscan-lumish-syndrome · Last refreshed: October 20, 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.

15w ago · JhealdBatch bot · 2026-07-04 view diff on Wikidata ↗

Mondo id → MONDO_0014791

Imported from → —

Umls cui → C4085873

Uniprot disease id → DI-04661

+ 6 other properties edited (see Wikidata diff for full list)

"/* wbeditentity-update:0| */ QuickStatements 3.0 [[:toollabs:qs-dev/batch/39873|batch #39873]]: P31 = "type of disease""

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