autosomal dominant nonsyndromic deafness 13

autosomal dominant nonsyndromic deafness that is characterized by postlingual onset in the second decade of life with mid-frequency hearing loss and has material basis in mutation in the COL11A2 gene on chromosome 6p21

MedicalCondition head_and_neck_disease Q28024672

Press Enter · cited answer in seconds

Summary

autosomal dominant nonsyndromic deafness 13 is a head and neck disease^[1].

Key Facts

autosomal dominant nonsyndromic deafness 13's instance of is recorded as head and neck disease^[2].
autosomal dominant nonsyndromic deafness 13's instance of is recorded as rare disease^[3].
autosomal dominant nonsyndromic deafness 13's instance of is recorded as class of disease^[4].
autosomal dominant nonsyndromic deafness 13 is a type of autosomal dominant nonsyndromic deafness^[5].
autosomal dominant nonsyndromic deafness 13's genetic association is recorded as COL11A2^[6].
autosomal dominant nonsyndromic deafness 13's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0110545^[7].
autosomal dominant nonsyndromic deafness 13's exact match is recorded as http://identifiers.org/doid/DOID:0110545^[8].
autosomal dominant nonsyndromic deafness 13's on focus list of Wikimedia project is recorded as WikiProject Medicine^[9].

⭐ Popularity Graph

0/100 long tail

Quick Facts

Instance of rare disease, class of disease

Subclass of autosomal dominant nonsyndromic deafness, head and neck disease

Properties

Exact match purl.obolibrary.org, identifiers.org

Genetic association COL11A2

On focus list of wikimedia project WikiProject Medicine

External References (7)

Disease ontology id DOID:0110545

Icd-10-cm H90.3

Mesh descriptor id C566612

Mondo id MONDO_0011159

Omim id 601868

Umls cui C1866095

Uniprot disease id DI-00843

🏷️ Also known as

en autosomal dominant deafness 13 en autosomal dominant nonsyndromic deafness 13 en autosomal dominant nonsyndromic deafness type 13 en DEAFNESS, AUTOSOMAL DOMINANT 13 en DEAFNESS, AUTOSOMAL DOMINANT 13; DFNA13 en Deafness, Autosomal Dominant type 13 en DFNA13

References

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

Direct Wikidata claims

[2] ↑ autosomal dominant nonsyndromic deafness 13 — instance of (P31): head and neck disease. Monarch Disease Ontology release 2018-06-29. Retrieved 2018-07-28. wikidata.org.
[3] ↑ autosomal dominant nonsyndromic deafness 13 — instance of (P31): rare disease. wikidata.org.
[4] ↑ autosomal dominant nonsyndromic deafness 13 — instance of (P31): class of disease. wikidata.org.
[5] ↑ autosomal dominant nonsyndromic deafness 13 — subclass of (P279): autosomal dominant nonsyndromic deafness. Disease Ontology. Retrieved 2020-11-30. wikidata.org.
[6] ↑ autosomal dominant nonsyndromic deafness 13 — genetic association (P2293): COL11A2. UniProt. Retrieved 2019-08-13. wikidata.org.
[7] ↑ autosomal dominant nonsyndromic deafness 13 — exact match (P2888): http://purl.obolibrary.org/obo/DOID_0110545. Disease Ontology. Retrieved 2020-11-30. wikidata.org.
[8] ↑ autosomal dominant nonsyndromic deafness 13 — exact match (P2888): http://identifiers.org/doid/DOID:0110545. Identifiers.org. registry.identifiers.org. Provenance: wikidata.org.
[9] ↑ autosomal dominant nonsyndromic deafness 13 — on focus list of Wikimedia project (P5008): WikiProject Medicine. wikidata.org.

Class ancestry

[1] ↑ autosomal dominant nonsyndromic deafness 13 is an instance of head and neck disease (Q55789477) [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 nonsyndromic deafness 13. Retrieved May 3, 2026, from https://4ort.xyz/entity/autosomal-dominant-nonsyndromic-deafness-13

MLA

“autosomal dominant nonsyndromic deafness 13.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/autosomal-dominant-nonsyndromic-deafness-13.

BibTeX

@misc{4ortxyz_autosomal-dominant-nonsyndromic-deafness-13_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{autosomal dominant nonsyndromic deafness 13}}, year = {2026}, url = {https://4ort.xyz/entity/autosomal-dominant-nonsyndromic-deafness-13}, note = {Accessed: 2026-05-03}}

LLM prompt

According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): autosomal dominant nonsyndromic deafness 13 — https://4ort.xyz/entity/autosomal-dominant-nonsyndromic-deafness-13 (retrieved 2026-05-03)

Canonical URL: https://4ort.xyz/entity/autosomal-dominant-nonsyndromic-deafness-13 · 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.

15w ago · JhealdBatch bot · 2026-07-03 view diff on Wikidata ↗

Mondo id → MONDO_0011159

Genetic association → COL11A2

Instance of → head and neck disease, rare disease, class of disease

Imported from → —

+ 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"

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