Autosomal recessive nonsyndromic hearing loss 22

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

Also known as: autosomal recessive nonsyndromic hearing loss 22, DFNB22, OTOA autosomal recessive nonsyndromic deafness, autosomal recessive deafness 22, autosomal recessive nonsyndromic deafness 22, autosomal recessive nonsyndromic deafness caused by mutation in OTOA, autosomal recessive nonsyndromic deafness type 22, deafness, autosomal recessive 22

0 clinical trials for this condition and its sub-types, 0 tagged with Autosomal recessive nonsyndromic hearing loss 22 itself.