Luscan-Lumish syndrome

human disease

MedicalCondition rare_disease Q55785011

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Luscan-Lumish syndrome

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's subclass of is recorded as genetic disease^[4].
Luscan-Lumish syndrome's subclass of is recorded as Sotos syndrome^[5].
Luscan-Lumish syndrome's OMIM ID is recorded as 616831^[6].
Luscan-Lumish syndrome's KEGG ID is recorded as H02444^[7].
Luscan-Lumish syndrome's genetic association is recorded as SETD2^[8].
Luscan-Lumish syndrome's UMLS CUI is recorded as C4085873^[9].
Luscan-Lumish syndrome's Mondo ID is recorded as MONDO_0014791^[10].
Luscan-Lumish syndrome's UniProt disease ID is recorded as DI-04661^[11].

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Quick Facts

Instance of rare disease, disease

Subclass of genetic disease, Sotos syndrome

Properties

Genetic association SETD2

Imported from wholeness_audit_2026-05-02

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

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 — OMIM ID (P492): 616831. Monarch Disease Ontology release 2018-06-29. Retrieved 2018-07-28. wikidata.org.
[7] ↑ Luscan-Lumish syndrome — KEGG ID (P665): H02444. wikidata.org.
[8] ↑ 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.
[9] ↑ Luscan-Lumish syndrome — UMLS CUI (P2892): C4085873. Monarch Disease Ontology release 2018-06-29. Retrieved 2018-07-28. wikidata.org.
[10] ↑ Luscan-Lumish syndrome — Mondo ID (P5270): MONDO_0014791. wikidata.org.
[11] ↑ Luscan-Lumish syndrome — UniProt disease ID (P11430): DI-04661. wikidata.org.

Class ancestry

[1] ↑ Luscan-Lumish syndrome is an instance of rare disease (Q929833) [P31, primary]. Wikidata. wikidata.org.

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APA

4ort.xyz Knowledge Graph. (2026). Luscan-Lumish syndrome. Retrieved May 3, 2026, from https://4ort.xyz/entity/luscan-lumish-syndrome

MLA

“Luscan-Lumish syndrome.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 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: 2026-05-03}}

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 2026-05-03)

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