Autosomal recessive nonsyndromic hearing loss 18A

Any autosomal recessive nonsyndromic deafness in which the cause of the disease is a mutation in the USH1C gene.

Also known as: DFNB18A, USH1C autosomal recessive nonsyndromic deafness, autosomal recessive deafness 18A, autosomal recessive nonsyndromic deafness 18A, autosomal recessive nonsyndromic deafness caused by mutation in USH1C, autosomal recessive nonsyndromic deafness type 18A, deafness, autosomal recessive 18, deafness, autosomal recessive 18A

0 clinical trials for this condition and its sub-types, 0 tagged with Autosomal recessive nonsyndromic hearing loss 18A itself.