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autosomal dominant nonsyndromic deafness 22

autosomal dominant nonsyndromic deafness that is characterized by postlingual onset with high frequency progressive hearing loss and has material basis in mutation in the MYO6 gene on chromosome 6q14
MedicalCondition developmental_defect_during_embryogenesis Q28024680
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autosomal dominant nonsyndromic deafness 22

Summary

autosomal dominant nonsyndromic deafness 22 is a developmental defect during embryogenesis[1].

Key Facts

  • autosomal dominant nonsyndromic deafness 22's instance of is recorded as developmental defect during embryogenesis[2].
  • autosomal dominant nonsyndromic deafness 22's instance of is recorded as head and neck disease[3].
  • autosomal dominant nonsyndromic deafness 22's instance of is recorded as rare disease[4].
  • autosomal dominant nonsyndromic deafness 22's instance of is recorded as class of disease[5].
  • autosomal dominant nonsyndromic deafness 22's subclass of is recorded as autosomal dominant nonsyndromic deafness[6].
  • autosomal dominant nonsyndromic deafness 22's subclass of is recorded as syndromic genetic deafness[7].
  • autosomal dominant nonsyndromic deafness 22's subclass of is recorded as syndrome associated with hypertrophic cardiomyopathy[8].
  • autosomal dominant nonsyndromic deafness 22's subclass of is recorded as genetic cardiac rhythm disease[9].
  • autosomal dominant nonsyndromic deafness 22's OMIM ID is recorded as 606346[10].
  • autosomal dominant nonsyndromic deafness 22's Disease Ontology ID is recorded as DOID:0110552[11].
  • autosomal dominant nonsyndromic deafness 22's Orphanet ID is recorded as 228012[12].
  • autosomal dominant nonsyndromic deafness 22's genetic association is recorded as MYO6[13].
  • autosomal dominant nonsyndromic deafness 22's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0110552[14].
  • autosomal dominant nonsyndromic deafness 22's exact match is recorded as http://identifiers.org/doid/DOID:0110552[15].
  • autosomal dominant nonsyndromic deafness 22's UMLS CUI is recorded as C4304831[16].
  • autosomal dominant nonsyndromic deafness 22's ICD-10-CM is recorded as H90.3[17].
  • autosomal dominant nonsyndromic deafness 22's GARD rare disease ID is recorded as 9167[18].
  • autosomal dominant nonsyndromic deafness 22's on focus list of Wikimedia project is recorded as WikiProject Medicine[19].
  • autosomal dominant nonsyndromic deafness 22's Mondo ID is recorded as MONDO_0016424[20].
  • autosomal dominant nonsyndromic deafness 22's UniProt disease ID is recorded as DI-00847[21].

References

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

Direct Wikidata claims

  1. [2] ↑ . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  2. [3] ↑ . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  3. [4] ↑ . wikidata.org.
  4. [5] ↑ . wikidata.org.
  5. [6] ↑ . Disease Ontology. Retrieved . wikidata.org.
  6. [7] ↑ . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  7. [8] ↑ . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  8. [9] ↑ . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  9. [10] ↑ . Disease Ontology. Retrieved . wikidata.org.
  10. [11] ↑ . Disease Ontology. Retrieved . wikidata.org.
  11. [12] ↑ . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  12. [13] ↑ . Novel association of hypertrophic cardiomyopathy, sensorineural deafness, and a mutation in unconventional myosin VI (MYO6).. Retrieved . platform.opentargets.org. Provenance: wikidata.org.
  13. [14] ↑ . Disease Ontology. Retrieved . wikidata.org.
  14. [15] ↑ . Identifiers.org. registry.identifiers.org. Provenance: wikidata.org.
  15. [16] ↑ . UMLS 2023. Retrieved . wikidata.org.
  16. [17] ↑ . Disease Ontology. Retrieved . wikidata.org.
  17. [18] ↑ . wikidata.org.
  18. [19] ↑ . wikidata.org.
  19. [20] ↑ . wikidata.org.
  20. [21] ↑ . wikidata.org.

Class ancestry

  1. [1] ↑ . Wikidata. wikidata.org.

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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 22. Retrieved May 3, 2026, from https://4ort.xyz/entity/autosomal-dominant-nonsyndromic-deafness-22
MLA “autosomal dominant nonsyndromic deafness 22.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/autosomal-dominant-nonsyndromic-deafness-22.
BibTeX @misc{4ortxyz_autosomal-dominant-nonsyndromic-deafness-22_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{autosomal dominant nonsyndromic deafness 22}}, year = {2026}, url = {https://4ort.xyz/entity/autosomal-dominant-nonsyndromic-deafness-22}, note = {Accessed: 2026-05-03}}
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