Autosomal recessive nonsyndromic hearing loss 79

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

Also known as: autosomal recessive nonsyndromic hearing loss 79, DFNB79, TPRN autosomal recessive nonsyndromic deafness, autosomal recessive deafness 79, autosomal recessive nonsyndromic deafness 79, autosomal recessive nonsyndromic deafness caused by mutation in TPRN, autosomal recessive nonsyndromic deafness type 79, deafness, autosomal recessive 79

0 clinical trials for this condition and its sub-types, 0 tagged with Autosomal recessive nonsyndromic hearing loss 79 itself.