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autosomal recessive nonsyndromic deafness 12

autosomal recessive nonsyndromic deafness that is characterized by prelingual onset with severe to profound, stable hearing loss and has material basis in mutation in the CDH23 gene on chromosome 10q22
MedicalCondition head_and_neck_disease Q28024592
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autosomal recessive nonsyndromic deafness 12

Summary

autosomal recessive nonsyndromic deafness 12 is a head and neck disease[1].

Key Facts

  • autosomal recessive nonsyndromic deafness 12's instance of is recorded as head and neck disease[2].
  • autosomal recessive nonsyndromic deafness 12's instance of is recorded as rare disease[3].
  • autosomal recessive nonsyndromic deafness 12's instance of is recorded as class of disease[4].
  • autosomal recessive nonsyndromic deafness 12's subclass of is recorded as autosomal recessive nonsyndromic deafness[5].
  • autosomal recessive nonsyndromic deafness 12's MeSH descriptor ID is recorded as C563327[6].
  • autosomal recessive nonsyndromic deafness 12's OMIM ID is recorded as 601386[7].
  • autosomal recessive nonsyndromic deafness 12's Disease Ontology ID is recorded as DOID:0110467[8].
  • autosomal recessive nonsyndromic deafness 12's NCI Thesaurus ID is recorded as C201586[9].
  • autosomal recessive nonsyndromic deafness 12's genetic association is recorded as CDH23[10].
  • autosomal recessive nonsyndromic deafness 12's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0110467[11].
  • autosomal recessive nonsyndromic deafness 12's exact match is recorded as http://identifiers.org/doid/DOID:0110467[12].
  • autosomal recessive nonsyndromic deafness 12's UMLS CUI is recorded as C1832394[13].
  • autosomal recessive nonsyndromic deafness 12's ICD-10-CM is recorded as H90.3[14].
  • autosomal recessive nonsyndromic deafness 12's on focus list of Wikimedia project is recorded as WikiProject Medicine[15].
  • autosomal recessive nonsyndromic deafness 12's Mondo ID is recorded as MONDO_0011067[16].
  • autosomal recessive nonsyndromic deafness 12's UniProt disease ID is recorded as DI-00862[17].

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] ↑ . wikidata.org.
  3. [4] ↑ . wikidata.org.
  4. [5] ↑ . Disease Ontology. Retrieved . wikidata.org.
  5. [6] ↑ . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  6. [7] ↑ . Disease Ontology. Retrieved . wikidata.org.
  7. [8] ↑ . Disease Ontology. Retrieved . wikidata.org.
  8. [9] ↑ . wikidata.org.
  9. [10] ↑ . Q905695. Retrieved . wikidata.org.
  10. [11] ↑ . Disease Ontology. Retrieved . wikidata.org.
  11. [12] ↑ . Identifiers.org. registry.identifiers.org. Provenance: wikidata.org.
  12. [13] ↑ . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  13. [14] ↑ . Disease Ontology. Retrieved . wikidata.org.
  14. [15] ↑ . wikidata.org.
  15. [16] ↑ . wikidata.org.
  16. [17] ↑ . 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.

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MLA “autosomal recessive nonsyndromic deafness 12.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/autosomal-recessive-nonsyndromic-deafness-12.
BibTeX @misc{4ortxyz_autosomal-recessive-nonsyndromic-deafness-12_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{autosomal recessive nonsyndromic deafness 12}}, year = {2026}, url = {https://4ort.xyz/entity/autosomal-recessive-nonsyndromic-deafness-12}, note = {Accessed: 2026-05-03}}
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