Variants
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Autosomal dominant nonsyndromic hearing loss 3B

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Description

Nonsyndromic hearing loss and deafness, DFNA3 is characterized by pre- or postlingual, mild-to-profound progressive high-frequency sensorineural hearing impairment. Affected individuals have no other associated medical findings.

GeneReviews

  • Mode of Inheritance

  • Autosomal dominant inheritance

VARIANTS

28

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Genes

External Links

  • OMIM

    612643

  • Orphanet
  • HPO
  • Medgen

    C2675237

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