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GTR Home > Conditions/Phenotypes > Autosomal recessive nonsyndromic hearing loss 2

Autosomal recessive nonsyndromic hearing loss 2

Synonyms
DFNB 2 Nonsyndromic Hearing Loss and Deafness; Deafness, autosomal recessive 2; NEUROSENSORY NONSYNDROMIC RECESSIVE DEAFNESS 2

Summary

Any autosomal recessive nonsyndromic deafness in which the cause of the disease is a mutation in the MYO7A gene. [from MONDO]

Available tests

50 tests are in the database for this condition.

Check Related conditions for additional relevant tests.

Clinical tests (50 available)

Molecular Genetics Tests

Genes See tests for all associated and related genes

  • Also known as: DFNA11, DFNB2, MYOVIIA, MYU7A, NSRD2, USH1B, MYO7A
    Summary: myosin VIIA

Clinical features

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Imported from Human Phenotype Ontology (HPO)

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