Autosomal recessive nonsyndromic hearing loss 13
MONDO:0011286An autosomal recessive nonsyndromic deafness that has material basis in variation in the chromosome region 7q34-q36.
Also known as: DFNB13, autosomal recessive deafness 13, autosomal recessive nonsyndromic deafness 13, autosomal recessive nonsyndromic deafness type 13, deafness, autosomal recessive 13
60 clinical trials for this condition and its sub-types.
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