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GTR Home > Conditions/Phenotypes > Autosomal dominant nonsyndromic hearing loss 20

Autosomal dominant nonsyndromic hearing loss 20

Synonyms
DFNA20/26 Nonsyndromic Hearing Loss and Deafness; Deafness, autosomal dominant 20

Summary

Any autosomal dominant nonsyndromic deafness in which the cause of the disease is a mutation in the ACTG1 gene. [from MONDO]

Available tests

35 tests are in the database for this condition.

Check Related conditions for additional relevant tests.

Clinical tests (35 available)

Molecular Genetics Tests

Genes See tests for all associated and related genes

  • Also known as: ACT, ACTG, DFNA20, DFNA26, HEL-176, ACTG1
    Summary: actin gamma 1

Clinical features

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Imported from Human Phenotype Ontology (HPO)

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