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GTR Home > Conditions/Phenotypes > Autosomal recessive nonsyndromic hearing loss 49

Summary

Autosomal recessive deafness-49 (DFNB49) is characterized by prelingual profound sensorineural hearing loss at all frequencies (Riazuddin et al., 2006 and Chishti et al., 2008). [from OMIM]

Available tests

20 tests are in the database for this condition.

Check Related conditions for additional relevant tests.

Genes See tests for all associated and related genes

  • Also known as: DFNB49, MARVD2, MRVLDC2, Tric, MARVELD2
    Summary: MARVEL domain containing 2

Clinical features

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