autosomal recessive nonsyndromic deafness 101

autosomal recessive nonsyndromic deafness that has material basis in mutation in the GRXCR2 gene on chromosome 5q32

MedicalCondition rare_disease Q28024587

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Summary

autosomal recessive nonsyndromic deafness 101 is a rare disease^[1].

Key Facts

autosomal recessive nonsyndromic deafness 101's instance of is recorded as rare disease^[2].
autosomal recessive nonsyndromic deafness 101's instance of is recorded as class of disease^[3].
autosomal recessive nonsyndromic deafness 101's subclass of is recorded as autosomal recessive nonsyndromic deafness^[4].
autosomal recessive nonsyndromic deafness 101's OMIM ID is recorded as 615837^[5].
autosomal recessive nonsyndromic deafness 101's Disease Ontology ID is recorded as DOID:0110462^[6].
autosomal recessive nonsyndromic deafness 101's genetic association is recorded as GRXCR2^[7].
autosomal recessive nonsyndromic deafness 101's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0110462^[8].
autosomal recessive nonsyndromic deafness 101's exact match is recorded as http://identifiers.org/doid/DOID:0110462^[9].
autosomal recessive nonsyndromic deafness 101's UMLS CUI is recorded as C3892049^[10].
autosomal recessive nonsyndromic deafness 101's ICD-10-CM is recorded as H90.3^[11].
autosomal recessive nonsyndromic deafness 101's on focus list of Wikimedia project is recorded as WikiProject Medicine^[12].
autosomal recessive nonsyndromic deafness 101's Mondo ID is recorded as MONDO_0014363^[13].
autosomal recessive nonsyndromic deafness 101's UniProt disease ID is recorded as DI-04121^[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 GRXCR2

Imported from wholeness_audit_2026-05-02

On focus list of wikimedia project WikiProject Medicine

External References (6)

Disease ontology id DOID:0110462

Icd-10-cm H90.3

Mondo id MONDO_0014363

Omim id 615837

Umls cui C3892049

Uniprot disease id DI-04121

🏷️ Also known as

en autosomal recessive deafness 101 en autosomal recessive nonsyndromic deafness 101 en autosomal recessive nonsyndromic deafness type 101 en DEAFNESS, AUTOSOMAL RECESSIVE 101 en DEAFNESS, AUTOSOMAL RECESSIVE 101; DFNB101 en Deafness, Autosomal Recessive type 101 en DFNB101

References

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

Direct Wikidata claims

[2] ↑ autosomal recessive nonsyndromic deafness 101 — instance of (P31): rare disease. wikidata.org.
[3] ↑ autosomal recessive nonsyndromic deafness 101 — instance of (P31): class of disease. wikidata.org.
[4] ↑ autosomal recessive nonsyndromic deafness 101 — subclass of (P279): autosomal recessive nonsyndromic deafness. Disease Ontology. Retrieved 2020-11-30. wikidata.org.
[5] ↑ autosomal recessive nonsyndromic deafness 101 — OMIM ID (P492): 615837. Monarch Disease Ontology release 2018-06-29. Retrieved 2018-08-07. wikidata.org.
[6] ↑ autosomal recessive nonsyndromic deafness 101 — Disease Ontology ID (P699): DOID:0110462. Disease Ontology. Retrieved 2020-11-30. wikidata.org.
[7] ↑ autosomal recessive nonsyndromic deafness 101 — genetic association (P2293): GRXCR2. UniProt. Retrieved 2019-08-13. wikidata.org.
[8] ↑ autosomal recessive nonsyndromic deafness 101 — exact match (P2888): http://purl.obolibrary.org/obo/DOID_0110462. Disease Ontology. Retrieved 2020-11-30. wikidata.org.
[9] ↑ autosomal recessive nonsyndromic deafness 101 — exact match (P2888): http://identifiers.org/doid/DOID:0110462. Identifiers.org. registry.identifiers.org. Provenance: wikidata.org.
[10] ↑ autosomal recessive nonsyndromic deafness 101 — UMLS CUI (P2892): C3892049. Monarch Disease Ontology release 2018-06-29. Retrieved 2018-08-07. wikidata.org.
[11] ↑ autosomal recessive nonsyndromic deafness 101 — ICD-10-CM (P4229): H90.3. Disease Ontology. Retrieved 2019-08-28. wikidata.org.
[12] ↑ autosomal recessive nonsyndromic deafness 101 — on focus list of Wikimedia project (P5008): WikiProject Medicine. wikidata.org.
[13] ↑ autosomal recessive nonsyndromic deafness 101 — Mondo ID (P5270): MONDO_0014363. wikidata.org.
[14] ↑ autosomal recessive nonsyndromic deafness 101 — UniProt disease ID (P11430): DI-04121. wikidata.org.

Class ancestry

[1] ↑ autosomal recessive nonsyndromic deafness 101 is an instance of rare disease (Q929833) [P31, primary]. Wikidata. wikidata.org.

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APA

4ort.xyz Knowledge Graph. (2026). autosomal recessive nonsyndromic deafness 101. Retrieved May 3, 2026, from https://4ort.xyz/entity/autosomal-recessive-nonsyndromic-deafness-101

MLA

“autosomal recessive nonsyndromic deafness 101.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/autosomal-recessive-nonsyndromic-deafness-101.

BibTeX

@misc{4ortxyz_autosomal-recessive-nonsyndromic-deafness-101_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{autosomal recessive nonsyndromic deafness 101}}, year = {2026}, url = {https://4ort.xyz/entity/autosomal-recessive-nonsyndromic-deafness-101}, 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 101 — https://4ort.xyz/entity/autosomal-recessive-nonsyndromic-deafness-101 (retrieved 2026-05-03)

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