autosomal recessive nonsyndromic deafness 89

autosomal recessive nonsyndromic deafness that has material basis in mutation in the KARS gene on chromosome 16q23

MedicalCondition rare_disease Q28024661

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Summary

autosomal recessive nonsyndromic deafness 89 is a rare disease^[1].

Key Facts

autosomal recessive nonsyndromic deafness 89's instance of is recorded as rare disease^[2].
autosomal recessive nonsyndromic deafness 89's instance of is recorded as class of disease^[3].
autosomal recessive nonsyndromic deafness 89's subclass of is recorded as autosomal recessive nonsyndromic deafness^[4].
autosomal recessive nonsyndromic deafness 89's OMIM ID is recorded as 613916^[5].
autosomal recessive nonsyndromic deafness 89's Disease Ontology ID is recorded as DOID:0110534^[6].
autosomal recessive nonsyndromic deafness 89's genetic association is recorded as KARS1^[7].
autosomal recessive nonsyndromic deafness 89's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0110534^[8].
autosomal recessive nonsyndromic deafness 89's exact match is recorded as http://identifiers.org/doid/DOID:0110534^[9].
autosomal recessive nonsyndromic deafness 89's UMLS CUI is recorded as C3151351^[10].
autosomal recessive nonsyndromic deafness 89's ICD-10-CM is recorded as H90.3^[11].
autosomal recessive nonsyndromic deafness 89's on focus list of Wikimedia project is recorded as WikiProject Medicine^[12].
autosomal recessive nonsyndromic deafness 89's Mondo ID is recorded as MONDO_0013489^[13].
autosomal recessive nonsyndromic deafness 89's UniProt disease ID is recorded as DI-03865^[14].

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Quick Facts

Instance of rare disease, class of disease

Subclass of autosomal recessive nonsyndromic deafness

Properties

Exact match purl.obolibrary.org, identifiers.org

Genetic association KARS1

Imported from wholeness_audit_2026-05-02

On focus list of wikimedia project WikiProject Medicine

External References (6)

Disease ontology id DOID:0110534

Icd-10-cm H90.3

Mondo id MONDO_0013489

Omim id 613916

Umls cui C3151351

Uniprot disease id DI-03865

🏷️ Also known as

en autosomal recessive deafness 89 en autosomal recessive nonsyndromic deafness 89 en autosomal recessive nonsyndromic deafness type 89 en DEAFNESS, AUTOSOMAL RECESSIVE 89 en DEAFNESS, AUTOSOMAL RECESSIVE 89; DFNB89 en Deafness, Autosomal Recessive type 89 en DFNB89

References

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

Direct Wikidata claims

[2] ↑ autosomal recessive nonsyndromic deafness 89 — instance of (P31): rare disease. wikidata.org.
[3] ↑ autosomal recessive nonsyndromic deafness 89 — instance of (P31): class of disease. wikidata.org.
[4] ↑ autosomal recessive nonsyndromic deafness 89 — subclass of (P279): autosomal recessive nonsyndromic deafness. Disease Ontology. Retrieved 2021-11-29. wikidata.org.
[5] ↑ autosomal recessive nonsyndromic deafness 89 — OMIM ID (P492): 613916. Monarch Disease Ontology release 2018-06-29. Retrieved 2018-08-07. wikidata.org.
[6] ↑ autosomal recessive nonsyndromic deafness 89 — Disease Ontology ID (P699): DOID:0110534. Disease Ontology. Retrieved 2021-11-29. wikidata.org.
[7] ↑ autosomal recessive nonsyndromic deafness 89 — genetic association (P2293): KARS1. UniProt. Retrieved 2019-08-13. wikidata.org.
[8] ↑ autosomal recessive nonsyndromic deafness 89 — exact match (P2888): http://purl.obolibrary.org/obo/DOID_0110534. Disease Ontology. Retrieved 2021-11-29. wikidata.org.
[9] ↑ autosomal recessive nonsyndromic deafness 89 — exact match (P2888): http://identifiers.org/doid/DOID:0110534. Identifiers.org. registry.identifiers.org. Provenance: wikidata.org.
[10] ↑ autosomal recessive nonsyndromic deafness 89 — UMLS CUI (P2892): C3151351. Monarch Disease Ontology release 2018-06-29. Retrieved 2018-08-07. wikidata.org.
[11] ↑ autosomal recessive nonsyndromic deafness 89 — ICD-10-CM (P4229): H90.3. Disease Ontology. Retrieved 2019-08-28. wikidata.org.
[12] ↑ autosomal recessive nonsyndromic deafness 89 — on focus list of Wikimedia project (P5008): WikiProject Medicine. wikidata.org.
[13] ↑ autosomal recessive nonsyndromic deafness 89 — Mondo ID (P5270): MONDO_0013489. wikidata.org.
[14] ↑ autosomal recessive nonsyndromic deafness 89 — UniProt disease ID (P11430): DI-03865. wikidata.org.

Class ancestry

[1] ↑ autosomal recessive nonsyndromic deafness 89 is an instance of rare disease (Q929833) [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 89. Retrieved May 3, 2026, from https://4ort.xyz/entity/autosomal-recessive-nonsyndromic-deafness-89

MLA

“autosomal recessive nonsyndromic deafness 89.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/autosomal-recessive-nonsyndromic-deafness-89.

BibTeX

@misc{4ortxyz_autosomal-recessive-nonsyndromic-deafness-89_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{autosomal recessive nonsyndromic deafness 89}}, year = {2026}, url = {https://4ort.xyz/entity/autosomal-recessive-nonsyndromic-deafness-89}, 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 89 — https://4ort.xyz/entity/autosomal-recessive-nonsyndromic-deafness-89 (retrieved 2026-05-03)

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