Autosomal recessive nonsyndromic hearing loss 59

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

Also known as: autosomal recessive nonsyndromic hearing loss 59, DFNB59, PJVK autosomal recessive nonsyndromic deafness, autosomal recessive deafness 59, autosomal recessive nonsyndromic deafness 59, autosomal recessive nonsyndromic deafness caused by mutation in PJVK, autosomal recessive nonsyndromic deafness type 59, deafness, autosomal recessive 59

0 clinical trials for this condition and its sub-types, 0 tagged with Autosomal recessive nonsyndromic hearing loss 59 itself.