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's subclass of is recorded as autosomal recessive nonsyndromic deafness^[5].
autosomal recessive nonsyndromic deafness 2's MeSH descriptor ID is recorded as C564007^[6].
autosomal recessive nonsyndromic deafness 2's OMIM ID is recorded as 600060^[7].
autosomal recessive nonsyndromic deafness 2's Disease Ontology ID is recorded as DOID:0110477^[8].
autosomal recessive nonsyndromic deafness 2's genetic association is recorded as MYO7A^[9].
autosomal recessive nonsyndromic deafness 2's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0110477^[10].
autosomal recessive nonsyndromic deafness 2's exact match is recorded as http://identifiers.org/doid/DOID:0110477^[11].
autosomal recessive nonsyndromic deafness 2's UMLS CUI is recorded as C1838701^[12].
autosomal recessive nonsyndromic deafness 2's ICD-10-CM is recorded as H90.3^[13].
autosomal recessive nonsyndromic deafness 2's on focus list of Wikimedia project is recorded as WikiProject Medicine^[14].
autosomal recessive nonsyndromic deafness 2's Mondo ID is recorded as MONDO_0010807^[15].
autosomal recessive nonsyndromic deafness 2's UniProt disease ID is recorded as DI-00854^[16].

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Quick Facts

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

Subclass of autosomal recessive nonsyndromic deafness

Properties

Exact match purl.obolibrary.org, identifiers.org

Genetic association MYO7A

Imported from wholeness_audit_2026-05-02

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

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 — MeSH descriptor ID (P486): C564007. Monarch Disease Ontology release 2018-06-29. Retrieved 2018-07-28. wikidata.org.
[7] ↑ autosomal recessive nonsyndromic deafness 2 — OMIM ID (P492): 600060. Disease Ontology. Retrieved 2019-08-28. wikidata.org.
[8] ↑ autosomal recessive nonsyndromic deafness 2 — Disease Ontology ID (P699): DOID:0110477. Disease Ontology. Retrieved 2019-08-28. wikidata.org.
[9] ↑ autosomal recessive nonsyndromic deafness 2 — genetic association (P2293): MYO7A. Q905695. Retrieved 2019-08-13. wikidata.org.
[10] ↑ autosomal recessive nonsyndromic deafness 2 — exact match (P2888): http://purl.obolibrary.org/obo/DOID_0110477. Disease Ontology. Retrieved 2019-08-28. wikidata.org.
[11] ↑ autosomal recessive nonsyndromic deafness 2 — exact match (P2888): http://identifiers.org/doid/DOID:0110477. Identifiers.org. ebi.ac.uk. Provenance: wikidata.org.
[12] ↑ autosomal recessive nonsyndromic deafness 2 — UMLS CUI (P2892): C1838701. Monarch Disease Ontology release 2018-06-29. Retrieved 2018-07-28. wikidata.org.
[13] ↑ autosomal recessive nonsyndromic deafness 2 — ICD-10-CM (P4229): H90.3. Disease Ontology. Retrieved 2019-08-28. wikidata.org.
[14] ↑ autosomal recessive nonsyndromic deafness 2 — on focus list of Wikimedia project (P5008): WikiProject Medicine. wikidata.org.
[15] ↑ autosomal recessive nonsyndromic deafness 2 — Mondo ID (P5270): MONDO_0010807. wikidata.org.
[16] ↑ autosomal recessive nonsyndromic deafness 2 — UniProt disease ID (P11430): DI-00854. wikidata.org.

Class ancestry

[1] ↑ autosomal recessive nonsyndromic deafness 2 is an instance of head and neck disease (Q55789477) [P31, primary]. Wikidata. wikidata.org.

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APA

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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)

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