autosomal dominant non-syndromic intellectual disability 33

autosomal dominant non-syndromic intellectual disability that has material basis in an autosomal dominant mutation of DPP6 on chromosome 7q36.2

MedicalCondition developmental_defect_during_embryogenesis Q50349637

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autosomal dominant non-syndromic intellectual disability 33

Summary

autosomal dominant non-syndromic intellectual disability 33 is a developmental defect during embryogenesis^[1].

Key Facts

autosomal dominant non-syndromic intellectual disability 33's instance of is recorded as developmental defect during embryogenesis^[2].
autosomal dominant non-syndromic intellectual disability 33's instance of is recorded as rare disease^[3].
autosomal dominant non-syndromic intellectual disability 33's instance of is recorded as class of disease^[4].
autosomal dominant non-syndromic intellectual disability 33 is a type of autosomal dominant non-syndromic intellectual disability^[5].
autosomal dominant non-syndromic intellectual disability 33 is a type of non-syndromic central nervous system malformation^[6].
autosomal dominant non-syndromic intellectual disability 33's genetic association is recorded as DPP6^[7].
autosomal dominant non-syndromic intellectual disability 33's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0070063^[8].
autosomal dominant non-syndromic intellectual disability 33's exact match is recorded as http://identifiers.org/doid/DOID:0070063^[9].
autosomal dominant non-syndromic intellectual disability 33's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_2514^[10].
autosomal dominant non-syndromic intellectual disability 33's on focus list of Wikimedia project is recorded as WikiProject Medicine^[11].

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Quick Facts

Instance of rare disease, class of disease

Subclass of autosomal dominant non-syndromic intellectual disability, non-syndromic central nervous system malformation, developmental defect during embryogenesis

Properties

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

Genetic association DPP6

On focus list of wikimedia project WikiProject Medicine

External References (5)

Disease ontology id DOID:0070063

Mondo id MONDO_0014580

Omim id 616311

Umls cui C4225375

Uniprot disease id DI-04391

References

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

Direct Wikidata claims

[2] ↑ autosomal dominant non-syndromic intellectual disability 33 — 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 33 — instance of (P31): rare disease. wikidata.org.
[4] ↑ autosomal dominant non-syndromic intellectual disability 33 — instance of (P31): class of disease. wikidata.org.
[5] ↑ autosomal dominant non-syndromic intellectual disability 33 — subclass of (P279): autosomal dominant non-syndromic intellectual disability. Disease Ontology. Retrieved 2020-11-29. wikidata.org.
[6] ↑ autosomal dominant non-syndromic intellectual disability 33 — subclass of (P279): non-syndromic central nervous system malformation. Monarch Disease Ontology release 2018-06-29. Retrieved 2018-07-28. wikidata.org.
[7] ↑ autosomal dominant non-syndromic intellectual disability 33 — genetic association (P2293): DPP6. Q905695. Retrieved 2019-08-13. wikidata.org.
[8] ↑ autosomal dominant non-syndromic intellectual disability 33 — exact match (P2888): http://purl.obolibrary.org/obo/DOID_0070063. Disease Ontology. Retrieved 2020-11-29. wikidata.org.
[9] ↑ autosomal dominant non-syndromic intellectual disability 33 — exact match (P2888): http://identifiers.org/doid/DOID:0070063. Identifiers.org. registry.identifiers.org. Provenance: wikidata.org.
[10] ↑ autosomal dominant non-syndromic intellectual disability 33 — exact match (P2888): http://www.orpha.net/ORDO/Orphanet_2514. wikidata.org.
[11] ↑ autosomal dominant non-syndromic intellectual disability 33 — on focus list of Wikimedia project (P5008): WikiProject Medicine. wikidata.org.

Class ancestry

[1] ↑ autosomal dominant non-syndromic intellectual disability 33 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). autosomal dominant non-syndromic intellectual disability 33. Retrieved May 3, 2026, from https://4ort.xyz/entity/autosomal-dominant-non-syndromic-intellectual-disability-33

MLA

“autosomal dominant non-syndromic intellectual disability 33.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/autosomal-dominant-non-syndromic-intellectual-disability-33.

BibTeX

@misc{4ortxyz_autosomal-dominant-non-syndromic-intellectual-disability-33_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{autosomal dominant non-syndromic intellectual disability 33}}, year = {2026}, url = {https://4ort.xyz/entity/autosomal-dominant-non-syndromic-intellectual-disability-33}, 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 33 — https://4ort.xyz/entity/autosomal-dominant-non-syndromic-intellectual-disability-33 (retrieved 2026-05-03)

Canonical URL: https://4ort.xyz/entity/autosomal-dominant-non-syndromic-intellectual-disability-33 · 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.

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

Mondo id → MONDO_0014580

Genetic association → DPP6

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

Imported from → —

+ 8 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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