autosomal recessive nonsyndromic deafness 2

autosomal recessive nonsyndromic deafness that has material basis in mutation in the MYO7A gene on chromosome 11q13

MedicalCondition head_and_neck_disease Q28024602

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autosomal recessive nonsyndromic deafness 2

Summary

autosomal recessive nonsyndromic deafness 2 is a head and neck disease^[1].

Key Facts

autosomal recessive nonsyndromic deafness 2's instance of is recorded as head and neck disease^[2].
autosomal recessive nonsyndromic deafness 2's instance of is recorded as rare disease^[3].
autosomal recessive nonsyndromic deafness 2's instance of is recorded as class of disease^[4].
autosomal recessive nonsyndromic deafness 2 is a type of autosomal recessive nonsyndromic deafness^[5].
autosomal recessive nonsyndromic deafness 2's genetic association is recorded as MYO7A^[6].
autosomal recessive nonsyndromic deafness 2's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0110477^[7].
autosomal recessive nonsyndromic deafness 2's exact match is recorded as http://identifiers.org/doid/DOID:0110477^[8].
autosomal recessive nonsyndromic deafness 2'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 recessive nonsyndromic deafness, head and neck disease

Properties

Exact match purl.obolibrary.org, identifiers.org

Genetic association MYO7A

On focus list of wikimedia project WikiProject Medicine

External References (7)

Disease ontology id DOID:0110477

Icd-10-cm H90.3

Mesh descriptor id C564007

Mondo id MONDO_0010807

Omim id 600060

Umls cui C1838701

Uniprot disease id DI-00854

🏷️ Also known as

en autosomal recessive deafness 2 en autosomal recessive nonsyndromic deafness 2 en autosomal recessive nonsyndromic deafness type 2 en DEAFNESS, AUTOSOMAL RECESSIVE 2 en DEAFNESS, AUTOSOMAL RECESSIVE 2; DFNB2 en Deafness, Autosomal Recessive type 2 en DFNB2 en Neurosensory Nonsyndromic Recessive Deafness 2

References

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

Direct Wikidata claims

[2] ↑ autosomal recessive nonsyndromic deafness 2 — instance of (P31): head and neck disease. Monarch Disease Ontology release 2018-06-29. Retrieved 2018-07-28. wikidata.org.
[3] ↑ autosomal recessive nonsyndromic deafness 2 — instance of (P31): rare disease. wikidata.org.
[4] ↑ autosomal recessive nonsyndromic deafness 2 — instance of (P31): class of disease. wikidata.org.
[5] ↑ autosomal recessive nonsyndromic deafness 2 — subclass of (P279): autosomal recessive nonsyndromic deafness. Disease Ontology. Retrieved 2019-05-15. wikidata.org.
[6] ↑ autosomal recessive nonsyndromic deafness 2 — genetic association (P2293): MYO7A. Q905695. Retrieved 2019-08-13. wikidata.org.
[7] ↑ autosomal recessive nonsyndromic deafness 2 — exact match (P2888): http://purl.obolibrary.org/obo/DOID_0110477. Disease Ontology. Retrieved 2019-08-28. wikidata.org.
[8] ↑ autosomal recessive nonsyndromic deafness 2 — exact match (P2888): http://identifiers.org/doid/DOID:0110477. Identifiers.org. ebi.ac.uk. Provenance: wikidata.org.
[9] ↑ autosomal recessive nonsyndromic deafness 2 — on focus list of Wikimedia project (P5008): WikiProject Medicine. wikidata.org.

Class ancestry

[1] ↑ autosomal recessive nonsyndromic deafness 2 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 recessive nonsyndromic deafness 2. Retrieved May 3, 2026, from https://4ort.xyz/entity/autosomal-recessive-nonsyndromic-deafness-2

MLA

“autosomal recessive nonsyndromic deafness 2.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/autosomal-recessive-nonsyndromic-deafness-2.

BibTeX

@misc{4ortxyz_autosomal-recessive-nonsyndromic-deafness-2_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{autosomal recessive nonsyndromic deafness 2}}, year = {2026}, url = {https://4ort.xyz/entity/autosomal-recessive-nonsyndromic-deafness-2}, note = {Accessed: 2026-05-03}}

LLM prompt

According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): autosomal recessive nonsyndromic deafness 2 — https://4ort.xyz/entity/autosomal-recessive-nonsyndromic-deafness-2 (retrieved 2026-05-03)

Canonical URL: https://4ort.xyz/entity/autosomal-recessive-nonsyndromic-deafness-2 · 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_0010807

Genetic association → MYO7A

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"

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