Autosomal recessive nonsyndromic hearing loss 68

Any autosomal recessive nonsyndromic deafness in which the cause of the disease is a mutation in the S1PR2 gene.

Also known as: autosomal recessive nonsyndromic hearing loss 68, DFNB68, S1PR2 autosomal recessive nonsyndromic deafness, autosomal recessive deafness 68, autosomal recessive nonsyndromic deafness 68, autosomal recessive nonsyndromic deafness caused by mutation in S1PR2, autosomal recessive nonsyndromic deafness type 68, deafness, autosomal recessive 68

0 clinical trials for this condition and its sub-types, 0 tagged with Autosomal recessive nonsyndromic hearing loss 68 itself.