Autosomal recessive nonsyndromic hearing loss 23

Any autosomal recessive nonsyndromic deafness in which the cause of the disease is a mutation in the PCDH15 gene.

Also known as: DFNB23, PCDH15 autosomal recessive nonsyndromic deafness, autosomal recessive deafness 23, autosomal recessive nonsyndromic deafness 23, autosomal recessive nonsyndromic deafness caused by mutation in PCDH15, autosomal recessive nonsyndromic deafness type 23, deafness, autosomal recessive 23, deafness, autosomal recessive type 23

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