autosomal dominant nonsyndromic deafness 17

autosomal dominant nonsyndromic deafness that is characterized by postlingual onset with high frequency progressive hearing loss and has material basis in mutation in the MYH9 gene on chromosome 22q12

MedicalCondition head_and_neck_disease Q28024676

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Summary

autosomal dominant nonsyndromic deafness 17 is a head and neck disease^[1].

Key Facts

autosomal dominant nonsyndromic deafness 17's instance of is recorded as head and neck disease^[2].
autosomal dominant nonsyndromic deafness 17's instance of is recorded as rare disease^[3].
autosomal dominant nonsyndromic deafness 17's instance of is recorded as class of disease^[4].
autosomal dominant nonsyndromic deafness 17 is a type of autosomal dominant nonsyndromic deafness^[5].
autosomal dominant nonsyndromic deafness 17's genetic association is recorded as MYH9^[6].
autosomal dominant nonsyndromic deafness 17's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0110548^[7].
autosomal dominant nonsyndromic deafness 17's exact match is recorded as http://identifiers.org/doid/DOID:0110548^[8].
autosomal dominant nonsyndromic deafness 17'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 MYH9

On focus list of wikimedia project WikiProject Medicine

External References (6)

Disease ontology id DOID:0110548

Icd-10-cm H90.3

Mondo id MONDO_0011350

Omim id 603622

Umls cui C1863660, C1863659

Uniprot disease id DI-00845

🏷️ Also known as

en autosomal dominant deafness 17 en autosomal dominant nonsyndromic deafness 17 en autosomal dominant nonsyndromic deafness type 17 en Cochleosaccular Degeneration en DEAFNESS, AUTOSOMAL DOMINANT 17 en DEAFNESS, AUTOSOMAL DOMINANT 17; DFNA17 en Deafness, Autosomal Dominant type 17 en DFNA17

References

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

Direct Wikidata claims

[2] ↑ autosomal dominant nonsyndromic deafness 17 — 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 17 — instance of (P31): rare disease. wikidata.org.
[4] ↑ autosomal dominant nonsyndromic deafness 17 — instance of (P31): class of disease. wikidata.org.
[5] ↑ autosomal dominant nonsyndromic deafness 17 — subclass of (P279): autosomal dominant nonsyndromic deafness. Disease Ontology. Retrieved 2020-11-29. wikidata.org.
[6] ↑ autosomal dominant nonsyndromic deafness 17 — genetic association (P2293): MYH9. UniProt. Retrieved 2019-08-13. wikidata.org.
[7] ↑ autosomal dominant nonsyndromic deafness 17 — exact match (P2888): http://purl.obolibrary.org/obo/DOID_0110548. Disease Ontology. Retrieved 2020-11-29. wikidata.org.
[8] ↑ autosomal dominant nonsyndromic deafness 17 — exact match (P2888): http://identifiers.org/doid/DOID:0110548. Identifiers.org. registry.identifiers.org. Provenance: wikidata.org.
[9] ↑ autosomal dominant nonsyndromic deafness 17 — on focus list of Wikimedia project (P5008): WikiProject Medicine. wikidata.org.

Class ancestry

[1] ↑ autosomal dominant nonsyndromic deafness 17 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 17. Retrieved May 3, 2026, from https://4ort.xyz/entity/autosomal-dominant-nonsyndromic-deafness-17

MLA

“autosomal dominant nonsyndromic deafness 17.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/autosomal-dominant-nonsyndromic-deafness-17.

BibTeX

@misc{4ortxyz_autosomal-dominant-nonsyndromic-deafness-17_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{autosomal dominant nonsyndromic deafness 17}}, year = {2026}, url = {https://4ort.xyz/entity/autosomal-dominant-nonsyndromic-deafness-17}, 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 17 — https://4ort.xyz/entity/autosomal-dominant-nonsyndromic-deafness-17 (retrieved 2026-05-03)

Canonical URL: https://4ort.xyz/entity/autosomal-dominant-nonsyndromic-deafness-17 · 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_0011350

Genetic association → MYH9

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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