Autosomal dominant nonsyndromic hearing loss 3A

MONDO:0011103

Any autosomal dominant nonsyndromic deafness in which the cause of the disease is a mutation in the GJB2 gene.

Also known as: DFNA3, DFNA3A, GJB2 autosomal dominant nonsyndromic deafness, NSRD1, autosomal dominant deafness 3A, autosomal dominant nonsyndromic deafness 3A, autosomal dominant nonsyndromic deafness caused by mutation in GJB2, autosomal dominant nonsyndromic deafness type 3A

0 clinical trials for this condition and its sub-types, 0 tagged with Autosomal dominant nonsyndromic hearing loss 3A itself.

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