autosomal dominant non-syndromic intellectual disability 26

autosomal dominant non-syndromic intellectual disability that has material basis in an autosomal dominant mutation of AUTS2 on chromosome 7q11.22

MedicalCondition developmental_defect_during_embryogenesis Q50349630

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autosomal dominant non-syndromic intellectual disability 26

Summary

autosomal dominant non-syndromic intellectual disability 26 is a developmental defect during embryogenesis^[1].

Key Facts

autosomal dominant non-syndromic intellectual disability 26's instance of is recorded as developmental defect during embryogenesis^[2].
autosomal dominant non-syndromic intellectual disability 26's instance of is recorded as rare disease^[3].
autosomal dominant non-syndromic intellectual disability 26's instance of is recorded as class of disease^[4].
autosomal dominant non-syndromic intellectual disability 26 is a type of autosomal dominant non-syndromic intellectual disability^[5].
autosomal dominant non-syndromic intellectual disability 26 is a type of multiple congenital anomalies/dysmorphic syndrome-intellectual disability^[6].
autosomal dominant non-syndromic intellectual disability 26 is a type of rare disease with autism^[7].
autosomal dominant non-syndromic intellectual disability 26 is a type of genetic syndromic intellectual disability^[8].
autosomal dominant non-syndromic intellectual disability 26's genetic association is recorded as AUTS2^[9].
autosomal dominant non-syndromic intellectual disability 26's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0070056^[10].
autosomal dominant non-syndromic intellectual disability 26's exact match is recorded as http://identifiers.org/doid/DOID:0070056^[11].
autosomal dominant non-syndromic intellectual disability 26's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_352490^[12].
autosomal dominant non-syndromic intellectual disability 26's on focus list of Wikimedia project is recorded as WikiProject Medicine^[13].

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Quick Facts

Instance of rare disease, class of disease

Subclass of autosomal dominant non-syndromic intellectual disability, multiple congenital anomalies/dysmorphic syndrome-intellectual disability, rare disease with autism, genetic syndromic intellectual disability, developmental defect during embryogenesis

Properties

Exact match purl.obolibrary.org, identifiers.org, www.orpha.net

Genetic association AUTS2

On focus list of wikimedia project WikiProject Medicine

External References (7)

Disease ontology id DOID:0070056

Icd-10-cm F84.1

Mondo id MONDO_0014361

Omim id 615834

Orphanet id 352490

Umls cui C4014435, C4749945

Uniprot disease id DI-04120

References

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

Direct Wikidata claims

[2] ↑ autosomal dominant non-syndromic intellectual disability 26 — instance of (P31): developmental defect during embryogenesis. Monarch Disease Ontology release 2018-06-29. Retrieved 2018-07-28. wikidata.org.
[3] ↑ autosomal dominant non-syndromic intellectual disability 26 — instance of (P31): rare disease. wikidata.org.
[4] ↑ autosomal dominant non-syndromic intellectual disability 26 — instance of (P31): class of disease. wikidata.org.
[5] ↑ autosomal dominant non-syndromic intellectual disability 26 — subclass of (P279): autosomal dominant non-syndromic intellectual disability. Disease Ontology. Retrieved 2020-11-30. wikidata.org.
[6] ↑ autosomal dominant non-syndromic intellectual disability 26 — subclass of (P279): multiple congenital anomalies/dysmorphic syndrome-intellectual disability. Monarch Disease Ontology release 2018-06-29. Retrieved 2018-07-28. wikidata.org.
[7] ↑ autosomal dominant non-syndromic intellectual disability 26 — subclass of (P279): rare disease with autism. Monarch Disease Ontology release 2018-06-29. Retrieved 2018-07-28. wikidata.org.
[8] ↑ autosomal dominant non-syndromic intellectual disability 26 — subclass of (P279): genetic syndromic intellectual disability. Monarch Disease Ontology release 2018-06-29. Retrieved 2018-07-28. wikidata.org.
[9] ↑ autosomal dominant non-syndromic intellectual disability 26 — genetic association (P2293): AUTS2. Q905695. Retrieved 2019-08-13. platform.opentargets.org. Provenance: wikidata.org.
[10] ↑ autosomal dominant non-syndromic intellectual disability 26 — exact match (P2888): http://purl.obolibrary.org/obo/DOID_0070056. Disease Ontology. Retrieved 2020-11-30. wikidata.org.
[11] ↑ autosomal dominant non-syndromic intellectual disability 26 — exact match (P2888): http://identifiers.org/doid/DOID:0070056. Identifiers.org. registry.identifiers.org. Provenance: wikidata.org.
[12] ↑ autosomal dominant non-syndromic intellectual disability 26 — exact match (P2888): http://www.orpha.net/ORDO/Orphanet_352490. wikidata.org.
[13] ↑ autosomal dominant non-syndromic intellectual disability 26 — on focus list of Wikimedia project (P5008): WikiProject Medicine. wikidata.org.

Class ancestry

[1] ↑ autosomal dominant non-syndromic intellectual disability 26 is an instance of developmental defect during embryogenesis (Q55788864) [P31, primary]. Wikidata. wikidata.org.

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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 26. Retrieved May 3, 2026, from https://4ort.xyz/entity/autosomal-dominant-non-syndromic-intellectual-disability-26

MLA

“autosomal dominant non-syndromic intellectual disability 26.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/autosomal-dominant-non-syndromic-intellectual-disability-26.

BibTeX

@misc{4ortxyz_autosomal-dominant-non-syndromic-intellectual-disability-26_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{autosomal dominant non-syndromic intellectual disability 26}}, year = {2026}, url = {https://4ort.xyz/entity/autosomal-dominant-non-syndromic-intellectual-disability-26}, 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 26 — https://4ort.xyz/entity/autosomal-dominant-non-syndromic-intellectual-disability-26 (retrieved 2026-05-03)

Canonical URL: https://4ort.xyz/entity/autosomal-dominant-non-syndromic-intellectual-disability-26 · 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.

1d ago · JhealdBatch bot · 2026-07-03 view diff on Wikidata ↗

Mondo id → MONDO_0014361

Genetic association → AUTS2

Orphanet id → 352490

Instance of → developmental defect during embryogenesis, rare disease, class of disease

+ 10 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"

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