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autosomal dominant nonsyndromic deafness 5

autosomal dominant nonsyndromic deafness that is characterized by postlingual onset in the first decade of life and high frequency progressive hearing loss and has material basis in mutation in the DFNA5 gene on chromosome 7p15
MedicalCondition head_and_neck_disease Q28024704
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Summary

autosomal dominant nonsyndromic deafness 5 is a head and neck disease[1]. It is known by 7 alternative names across languages and contexts.[2]

Key Facts

  • Instance of: rare disease[3], class of disease[4]
  • Subclass of: autosomal dominant nonsyndromic deafness[5]
  • Genetic association: GSDME[6]
  • Exact match: http://purl.obolibrary.org/obo/DOID_0110575[7], http://identifiers.org/doid/DOID:0110575[8]
  • On focus list of Wikimedia project: WikiProject Medicine[9]

References

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

Direct Wikidata claims

  1. [3] ↑ . wikidata.org.
  2. [4] ↑ . wikidata.org.
  3. [5] ↑ . Disease Ontology. Retrieved . wikidata.org.
  4. [6] ↑ . UniProt. Retrieved . wikidata.org.
  5. [7] ↑ . Disease Ontology. Retrieved . wikidata.org.
  6. [8] ↑ . Identifiers.org. registry.identifiers.org. Provenance: wikidata.org.
  7. [9] ↑ . 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). autosomal dominant nonsyndromic deafness 5. Retrieved May 3, 2026, from https://4ort.xyz/entity/autosomal-dominant-nonsyndromic-deafness-5
MLA “autosomal dominant nonsyndromic deafness 5.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/autosomal-dominant-nonsyndromic-deafness-5.
BibTeX @misc{4ortxyz_autosomal-dominant-nonsyndromic-deafness-5_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{autosomal dominant nonsyndromic deafness 5}}, year = {2026}, url = {https://4ort.xyz/entity/autosomal-dominant-nonsyndromic-deafness-5}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): autosomal dominant nonsyndromic deafness 5 — https://4ort.xyz/entity/autosomal-dominant-nonsyndromic-deafness-5 (retrieved 2026-05-03)

Canonical URL: https://4ort.xyz/entity/autosomal-dominant-nonsyndromic-deafness-5 · Last refreshed:

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. 15w ago · JhealdBatch bot · 2026-07-03 view diff on Wikidata ↗
    Mondo id → MONDO_0010973
    Genetic association → GSDME
    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"
Live feed via Wikidata EventStreams. New edits appear within minutes of being made on Wikidata.