Autosomal recessive nonsyndromic hearing loss 1B

Any autosomal recessive nonsyndromic deafness in which the cause of the disease is a mutation in the GJB6 gene.

Also known as: Autosomal recessive deafness type 1B, DFNB1B, GJB6 autosomal recessive nonsyndromic deafness, autosomal recessive deafness 1B, autosomal recessive nonsyndromic deafness 1B, autosomal recessive nonsyndromic deafness caused by mutation in GJB6, autosomal recessive nonsyndromic deafness type 1B, deafness, autosomal recessive 1B

0 clinical trials for this condition and its sub-types, 0 tagged with Autosomal recessive nonsyndromic hearing loss 1B itself.