nonsyndromic deafness

auditory system disease that is associated with permanent hearing loss caused by damage to structures in the inner ear and/or the middle ear, which is not associated with other signs and symptoms
MedicalCondition head_and_neck_disease Q9079046
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nonsyndromic deafness

Summary

nonsyndromic deafness is a head and neck disease[1]. It is known by 9 alternative names across languages and contexts.[2]

Key Facts

  • nonsyndromic deafness's instance of is recorded as head and neck disease[3].
  • nonsyndromic deafness's instance of is recorded as class of disease[4].
  • nonsyndromic deafness is a type of genetic deafness[5].
  • nonsyndromic deafness is a type of ear disease[6].
  • nonsyndromic deafness is a type of rare deafness[7].
  • nonsyndromic deafness's genetic association is recorded as WHRN[8].
  • nonsyndromic deafness's genetic association is recorded as USH1G[9].
  • nonsyndromic deafness's genetic association is recorded as TNC[10].
  • nonsyndromic deafness's genetic association is recorded as TPRN[11].
  • nonsyndromic deafness's genetic association is recorded as ACTG1[12].
  • nonsyndromic deafness's genetic association is recorded as CDH23[13].
  • nonsyndromic deafness's genetic association is recorded as CIB2[14].
  • nonsyndromic deafness's genetic association is recorded as CLDN14[15].
  • nonsyndromic deafness's genetic association is recorded as COCH[16].
  • nonsyndromic deafness's genetic association is recorded as ESPN[17].
  • nonsyndromic deafness's genetic association is recorded as ESRRB[18].
  • nonsyndromic deafness's genetic association is recorded as EYA4[19].
  • nonsyndromic deafness's genetic association is recorded as GIPC3[20].
  • nonsyndromic deafness's genetic association is recorded as GRXCR1[21].
  • nonsyndromic deafness's genetic association is recorded as ILDR1[22].
  • nonsyndromic deafness's genetic association is recorded as KCNQ4[23].
  • nonsyndromic deafness's genetic association is recorded as LHFPL5[24].
  • nonsyndromic deafness's genetic association is recorded as LOXHD1[25].
  • nonsyndromic deafness's genetic association is recorded as MARVELD2[26].
  • nonsyndromic deafness's genetic association is recorded as MYH14[27].

Why It Matters

nonsyndromic deafness is known by 9 alternative names across languages and contexts.[2]

References

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

Direct Wikidata claims

  1. [3] . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  2. [4] . wikidata.org.
  3. [5] . wikidata.org.
  4. [6] . Disease Ontology. Retrieved . wikidata.org.
  5. [7] . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  6. [8] . ClinGen. Retrieved . search.clinicalgenome.org. Provenance: wikidata.org.
  7. [9] . ClinGen. Retrieved . search.clinicalgenome.org. Provenance: wikidata.org.
  8. [10] . ClinGen. Retrieved . search.clinicalgenome.org. Provenance: wikidata.org.
  9. [11] . ClinGen. Retrieved . search.clinicalgenome.org. Provenance: wikidata.org.
  10. [12] . ClinGen. Retrieved . search.clinicalgenome.org. Provenance: wikidata.org.
  11. [13] . ClinGen. Retrieved . search.clinicalgenome.org. Provenance: wikidata.org.
  12. [14] . ClinGen. Retrieved . search.clinicalgenome.org. Provenance: wikidata.org.
  13. [15] . ClinGen. Retrieved . search.clinicalgenome.org. Provenance: wikidata.org.
  14. [16] . ClinGen. Retrieved . search.clinicalgenome.org. Provenance: wikidata.org.
  15. [17] . ClinGen. Retrieved . search.clinicalgenome.org. Provenance: wikidata.org.
  16. [18] . ClinGen. Retrieved . search.clinicalgenome.org. Provenance: wikidata.org.
  17. [19] . ClinGen. Retrieved . search.clinicalgenome.org. Provenance: wikidata.org.
  18. [20] . ClinGen. Retrieved . search.clinicalgenome.org. Provenance: wikidata.org.
  19. [21] . ClinGen. Retrieved . search.clinicalgenome.org. Provenance: wikidata.org.
  20. [22] . ClinGen. Retrieved . search.clinicalgenome.org. Provenance: wikidata.org.
  21. [23] . ClinGen. Retrieved . search.clinicalgenome.org. Provenance: wikidata.org.
  22. [24] . ClinGen. Retrieved . search.clinicalgenome.org. Provenance: wikidata.org.
  23. [25] . ClinGen. Retrieved . search.clinicalgenome.org. Provenance: wikidata.org.
  24. [26] . ClinGen. Retrieved . search.clinicalgenome.org. Provenance: wikidata.org.
  25. [27] . ClinGen. Retrieved . search.clinicalgenome.org. Provenance: wikidata.org.

Class ancestry

  1. [1] . Wikidata. wikidata.org.

Aggregate / graph-position facts

  1. [2] . Wikidata aliases. 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). nonsyndromic deafness. Retrieved May 3, 2026, from https://4ort.xyz/entity/nonsyndromic-deafness
MLA “nonsyndromic deafness.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/nonsyndromic-deafness.
BibTeX @misc{4ortxyz_nonsyndromic-deafness_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{nonsyndromic deafness}}, year = {2026}, url = {https://4ort.xyz/entity/nonsyndromic-deafness}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): nonsyndromic deafness — https://4ort.xyz/entity/nonsyndromic-deafness (retrieved 2026-05-03)

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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.

  1. 13d ago · JhealdBatch bot · 2026-07-03 view diff on Wikidata ↗
    Subclass of genetic deafness, ear disease, rare deafness
    Genetic association WHRN, USH1G, TNC +36
    Subclass of
    Instance of head and neck disease, class of disease
    + 3 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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