autosomal dominant non-syndromic intellectual disability 6

autosomal dominant non-syndromic intellectual disability that has material basis in an autosomal dominant mutation of GRIN2B on chromosome 12p13.1

MedicalCondition rare_disease Q50349610

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autosomal dominant non-syndromic intellectual disability 6

Summary

autosomal dominant non-syndromic intellectual disability 6 is a rare disease^[1].

Key Facts

autosomal dominant non-syndromic intellectual disability 6's instance of is recorded as rare disease^[2].
autosomal dominant non-syndromic intellectual disability 6's instance of is recorded as class of disease^[3].
autosomal dominant non-syndromic intellectual disability 6 is a type of autosomal dominant non-syndromic intellectual disability^[4].
autosomal dominant non-syndromic intellectual disability 6's genetic association is recorded as GRIN2B^[5].
autosomal dominant non-syndromic intellectual disability 6's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0070036^[6].
autosomal dominant non-syndromic intellectual disability 6's exact match is recorded as http://identifiers.org/doid/DOID:0070036^[7].
autosomal dominant non-syndromic intellectual disability 6's on focus list of Wikimedia project is recorded as WikiProject Medicine^[8].

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Quick Facts

Instance of rare disease, class of disease

Subclass of autosomal dominant non-syndromic intellectual disability

Properties

Exact match purl.obolibrary.org, identifiers.org

Genetic association GRIN2B

On focus list of wikimedia project WikiProject Medicine

External References (5)

Disease ontology id DOID:0070036

Mondo id MONDO_0013509

Omim id 613970

Umls cui C3151411

Uniprot disease id DI-03128

🌐 Available in 2 languages

enGRIN2B-related neurodevelopmental disorder fiGRIN2B-oireyhtymä

References

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

Direct Wikidata claims

[2] ↑ autosomal dominant non-syndromic intellectual disability 6 — instance of (P31): rare disease. wikidata.org.
[3] ↑ autosomal dominant non-syndromic intellectual disability 6 — instance of (P31): class of disease. wikidata.org.
[4] ↑ autosomal dominant non-syndromic intellectual disability 6 — subclass of (P279): autosomal dominant non-syndromic intellectual disability. Disease Ontology. Retrieved 2021-11-29. wikidata.org.
[5] ↑ autosomal dominant non-syndromic intellectual disability 6 — genetic association (P2293): GRIN2B. Q905695. Retrieved 2019-08-13. wikidata.org.
[6] ↑ autosomal dominant non-syndromic intellectual disability 6 — exact match (P2888): http://purl.obolibrary.org/obo/DOID_0070036. Disease Ontology. Retrieved 2021-11-29. wikidata.org.
[7] ↑ autosomal dominant non-syndromic intellectual disability 6 — exact match (P2888): http://identifiers.org/doid/DOID:0070036. Identifiers.org. registry.identifiers.org. Provenance: wikidata.org.
[8] ↑ autosomal dominant non-syndromic intellectual disability 6 — on focus list of Wikimedia project (P5008): WikiProject Medicine. wikidata.org.

Class ancestry

[1] ↑ autosomal dominant non-syndromic intellectual disability 6 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). autosomal dominant non-syndromic intellectual disability 6. Retrieved May 3, 2026, from https://4ort.xyz/entity/autosomal-dominant-non-syndromic-intellectual-disability-6

MLA

“autosomal dominant non-syndromic intellectual disability 6.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/autosomal-dominant-non-syndromic-intellectual-disability-6.

BibTeX

@misc{4ortxyz_autosomal-dominant-non-syndromic-intellectual-disability-6_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{autosomal dominant non-syndromic intellectual disability 6}}, year = {2026}, url = {https://4ort.xyz/entity/autosomal-dominant-non-syndromic-intellectual-disability-6}, note = {Accessed: 2026-05-03}}

LLM prompt

According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): autosomal dominant non-syndromic intellectual disability 6 — https://4ort.xyz/entity/autosomal-dominant-non-syndromic-intellectual-disability-6 (retrieved 2026-05-03)

Canonical URL: https://4ort.xyz/entity/autosomal-dominant-non-syndromic-intellectual-disability-6 · 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.

5d ago · MatSuBot bot · 2026-06-29 view diff on Wikidata ↗

Genetic association → GRIN2B

Uniprot disease id → DI-03128

Exact match → http://purl.obolibrary.org/obo/DOID_0070036, http://identifiers.org/doid/DOID:0070036

On focus list of wikimedia project → WikiProject Medicine

+ 8 other properties edited (see Wikidata diff for full list)

"/* wbeditentity-update-languages-short:0||fi, ha */ import labels from sitelinks"

Live feed via Wikidata EventStreams. New edits appear within minutes of being made on Wikidata.