Autosomal recessive nonsyndromic hearing loss 29

Any autosomal recessive nonsyndromic deafness in which the cause of the disease is a mutation in the CLDN14 gene.

Also known as: autosomal recessive nonsyndromic hearing loss 29, CLDN14 autosomal recessive nonsyndromic deafness, DFNB29, autosomal recessive deafness 29, autosomal recessive nonsyndromic deafness 29, autosomal recessive nonsyndromic deafness caused by mutation in CLDN14, autosomal recessive nonsyndromic deafness type 29, deafness, autosomal recessive 29

0 clinical trials for this condition and its sub-types, 0 tagged with Autosomal recessive nonsyndromic hearing loss 29 itself.