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GTR Home > Conditions/Phenotypes > Autosomal dominant nonsyndromic hearing loss 22

Autosomal dominant nonsyndromic hearing loss 22

Synonyms
Autosomal dominant nonsyndromic deafness 22; DFNA 22; DFNA22 Nonsyndromic Hearing Loss and Deafness; Deafness, autosomal dominant 22; Deafness, autosomal dominant nonsyndromic sensorineural 22

Summary

Any autosomal dominant nonsyndromic deafness in which the cause of the disease is a mutation in the MYO6 gene. [from MONDO]

Available tests

25 tests are in the database for this condition.

Check Related conditions for additional relevant tests.

Clinical tests (25 available)

Molecular Genetics Tests

Genes See tests for all associated and related genes

  • Also known as: DFNA22, DFNB37, MYO6
    Summary: myosin VI

Clinical features

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Imported from Human Phenotype Ontology (HPO)

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