Autosomal recessive nonsyndromic hearing loss 98

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

Also known as: autosomal recessive nonsyndromic hearing loss 98, DFNB98, TSPEAR autosomal recessive nonsyndromic deafness, autosomal recessive deafness 98, autosomal recessive nonsyndromic deafness 98, autosomal recessive nonsyndromic deafness caused by mutation in TSPEAR, autosomal recessive nonsyndromic deafness type 98, deafness, autosomal recessive 98

0 clinical trials for this condition and its sub-types, 0 tagged with Autosomal recessive nonsyndromic hearing loss 98 itself.