Autosomal recessive nonsyndromic hearing loss 31

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

Also known as: autosomal recessive nonsyndromic hearing loss 31, DFNB31, WHRN autosomal recessive nonsyndromic deafness, autosomal recessive deafness 31, autosomal recessive nonsyndromic deafness 31, autosomal recessive nonsyndromic deafness caused by mutation in WHRN, autosomal recessive nonsyndromic deafness type 31, deafness, autosomal recessive 31

0 clinical trials for this condition and its sub-types, 0 tagged with Autosomal recessive nonsyndromic hearing loss 31 itself.