Autosomal recessive nonsyndromic hearing loss 101

Any autosomal recessive nonsyndromic deafness in which the cause of the disease is a mutation in the GRXCR2 gene.

Also known as: DFNB101, GRXCR2 autosomal recessive nonsyndromic deafness, autosomal recessive deafness 101, autosomal recessive nonsyndromic deafness 101, autosomal recessive nonsyndromic deafness caused by mutation in GRXCR2, autosomal recessive nonsyndromic deafness type 101, deafness, autosomal recessive 101, deafness, autosomal recessive type 101

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