Autosomal recessive nonsyndromic hearing loss 61

Any autosomal recessive nonsyndromic deafness in which the cause of the disease is a mutation in the SLC26A5 gene.

Also known as: DFNB61, SLC26A5 autosomal recessive nonsyndromic deafness, autosomal recessive deafness 61, autosomal recessive nonsyndromic deafness 61, autosomal recessive nonsyndromic deafness caused by mutation in SLC26A5, autosomal recessive nonsyndromic deafness type 61, deafness, autosomal recessive 61, deafness, autosomal recessive type 61

0 clinical trials for this condition and its sub-types, 0 tagged with Autosomal recessive nonsyndromic hearing loss 61 itself.