Autosomal recessive nonsyndromic hearing loss 3

Synonyms: DFNB 3 Nonsyndromic Hearing Loss and Deafness; Deafness, autosomal recessive 3; NEUROSENSORY NONSYNDROMIC RECESSIVE DEAFNESS 3

Summary

Autosomal recessive deafness-3 (DFNB3) is a congenital, profound, neurosensory deafness. There are no apparent vestibular abnormalities or dysmorphic features (Friedman et al., 1995). [from OMIM]

Available tests

20 tests are in the database for this condition.

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Clinical tests (20 available)

Molecular Genetics Tests

Genes See tests for all associated and related genes

Associated genes Help
Genes reported to contribute to the condition.

MYO15A
44 tests
Also known as: DFNB3, MYO15, MYO15A
Summary: myosin XVA

Imported from Human Phenotype Ontology (HPO)

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Ear malformation
- Profound sensorineural hearing impairment
  Profound sensorineural hearing impairment
  - MedGen UID: 868926
  - Concept ID: C4023338
  - Finding: Disease or Syndrome
  Ear malformation
  See: Feature record | Search on this feature

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