Autosomal recessive nonsyndromic hearing loss 48

Any autosomal recessive nonsyndromic deafness in which the cause of the disease is a mutation in the CIB2 gene.

Also known as: USH1J, Usher syndrome type 1J, autosomal recessive nonsyndromic hearing loss 48, CIB2 autosomal recessive nonsyndromic deafness, DFNB48, autosomal recessive nonsyndromic deafness caused by mutation in CIB2, autosomal recessive nonsyndromic deafness type 48, deafness, autosomal recessive 48

0 clinical trials for this condition and its sub-types, 0 tagged with Autosomal recessive nonsyndromic hearing loss 48 itself.