autosomal dominant nonsyndromic deafness 56

autosomal dominant nonsyndromic deafness that has material basis in mutation in the TNC gene on chromosome 9q33

MedicalCondition head_and_neck_disease Q28024710

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autosomal dominant nonsyndromic deafness 56

Summary

autosomal dominant nonsyndromic deafness 56 is a head and neck disease^[1].

Key Facts

autosomal dominant nonsyndromic deafness 56's instance of is recorded as head and neck disease^[2].
autosomal dominant nonsyndromic deafness 56's instance of is recorded as rare disease^[3].
autosomal dominant nonsyndromic deafness 56's instance of is recorded as class of disease^[4].
autosomal dominant nonsyndromic deafness 56 is a type of autosomal dominant nonsyndromic deafness^[5].
autosomal dominant nonsyndromic deafness 56's genetic association is recorded as TNC^[6].
autosomal dominant nonsyndromic deafness 56's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0110581^[7].
autosomal dominant nonsyndromic deafness 56's exact match is recorded as http://identifiers.org/doid/DOID:0110581^[8].
autosomal dominant nonsyndromic deafness 56's on focus list of Wikimedia project is recorded as WikiProject Medicine^[9].

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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 TNC

On focus list of wikimedia project WikiProject Medicine

External References (6)

Disease ontology id DOID:0110581

Icd-10-cm H90.3

Mondo id MONDO_0014283

Omim id 615629

Umls cui C3810170

Uniprot disease id DI-04030

🏷️ Also known as

en autosomal dominant deafness 56 en autosomal dominant nonsyndromic deafness 56 en autosomal dominant nonsyndromic deafness type 56 en DEAFNESS, AUTOSOMAL DOMINANT 56 en DEAFNESS, AUTOSOMAL DOMINANT 56; DFNA56 en Deafness, Autosomal Dominant type 56 en DFNA56

References

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

Direct Wikidata claims

[2] ↑ autosomal dominant nonsyndromic deafness 56 — 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 56 — instance of (P31): rare disease. wikidata.org.
[4] ↑ autosomal dominant nonsyndromic deafness 56 — instance of (P31): class of disease. wikidata.org.
[5] ↑ autosomal dominant nonsyndromic deafness 56 — subclass of (P279): autosomal dominant nonsyndromic deafness. Disease Ontology. Retrieved 2020-11-29. wikidata.org.
[6] ↑ autosomal dominant nonsyndromic deafness 56 — genetic association (P2293): TNC. Q905695. Retrieved 2019-08-13. wikidata.org.
[7] ↑ autosomal dominant nonsyndromic deafness 56 — exact match (P2888): http://purl.obolibrary.org/obo/DOID_0110581. Disease Ontology. Retrieved 2020-11-29. wikidata.org.
[8] ↑ autosomal dominant nonsyndromic deafness 56 — exact match (P2888): http://identifiers.org/doid/DOID:0110581. Identifiers.org. registry.identifiers.org. Provenance: wikidata.org.
[9] ↑ autosomal dominant nonsyndromic deafness 56 — on focus list of Wikimedia project (P5008): WikiProject Medicine. wikidata.org.

Class ancestry

[1] ↑ autosomal dominant nonsyndromic deafness 56 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 56. Retrieved May 3, 2026, from https://4ort.xyz/entity/autosomal-dominant-nonsyndromic-deafness-56

MLA

“autosomal dominant nonsyndromic deafness 56.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/autosomal-dominant-nonsyndromic-deafness-56.

BibTeX

@misc{4ortxyz_autosomal-dominant-nonsyndromic-deafness-56_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{autosomal dominant nonsyndromic deafness 56}}, year = {2026}, url = {https://4ort.xyz/entity/autosomal-dominant-nonsyndromic-deafness-56}, 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 56 — https://4ort.xyz/entity/autosomal-dominant-nonsyndromic-deafness-56 (retrieved 2026-05-03)

Canonical URL: https://4ort.xyz/entity/autosomal-dominant-nonsyndromic-deafness-56 · 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.

8w ago · JhealdBatch bot · 2026-07-03 view diff on Wikidata ↗

Mondo id → MONDO_0014283

Genetic association → TNC

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

Imported from → —

+ 9 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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