Autosomal recessive nonsyndromic hearing loss 16

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

Also known as: autosomal recessive nonsyndromic hearing loss 16, DFNB16, STRC autosomal recessive nonsyndromic deafness, autosomal recessive deafness 16, autosomal recessive nonsyndromic deafness 16, autosomal recessive nonsyndromic deafness caused by mutation in STRC, autosomal recessive nonsyndromic deafness type 16, deafness, autosomal recessive 16

60 clinical trials for this condition and its sub-types.