Autosomal recessive nonsyndromic hearing loss 93

Any autosomal recessive nonsyndromic deafness in which the cause of the disease is a mutation in the CABP2 gene.

Also known as: autosomal recessive nonsyndromic hearing loss 93, CABP2 autosomal recessive nonsyndromic deafness, DFNB93, autosomal recessive deafness 93, autosomal recessive nonsyndromic deafness 93, autosomal recessive nonsyndromic deafness caused by mutation in CABP2, autosomal recessive nonsyndromic deafness type 93, deafness, autosomal recessive 93

61 clinical trials for this condition and its sub-types.