Autosomal recessive nonsyndromic hearing loss 102

Any autosomal recessive nonsyndromic deafness in which the cause of the disease is a mutation in the EPS8 gene.

Also known as: autosomal recessive nonsyndromic hearing loss 102, DFNB102, EPS8 autosomal recessive nonsyndromic deafness, autosomal recessive deafness 102, autosomal recessive nonsyndromic deafness 102, autosomal recessive nonsyndromic deafness caused by mutation in EPS8, autosomal recessive nonsyndromic deafness type 102, deafness, autosomal recessive 102

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