Autosomal dominant nonsyndromic hearing loss 15

Synonyms: DEAFNESS, AUTOSOMAL DOMINANT 52; DFNA15 Nonsyndromic Hearing Loss and Deafness; Deafness, autosomal dominant 15

Summary

Autosomal dominant deafness-15 (DFNA15) is a form of progressive nonsyndromic sensorineural hearing loss with postlingual onset between the second and sixth decades of life (summary by Kim et al., 2013). [from OMIM]

Available tests

21 tests are in the database for this condition.

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Clinical tests (21 available)

Molecular Genetics Tests

Genes See tests for all associated and related genes

Associated genes Help
Genes reported to contribute to the condition.

POU4F3
37 tests
Also known as: BRN3C, DFNA15, DFNA42, DFNA52, POU4F3
Summary: POU class 4 homeobox 3

Imported from Human Phenotype Ontology (HPO)

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Ear malformation
- Hearing impairment
  Hearing impairment
  - MedGen UID: 235586
  - Concept ID: C1384666
  - Finding: Disease or Syndrome
  Ear malformation
  See: Feature record | Search on this feature

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