Autosomal recessive nonsyndromic hearing loss 5

MONDO:0000912

An autosomal recessive nonsyndromic deafness that has material basis in variation in the chromosome region 14q12.

Also known as: DFNB5, autosomal recessive deafness 5, autosomal recessive nonsyndromic deafness 5, autosomal recessive nonsyndromic deafness type 5, deafness, autosomal recessive 5, neurosensory nonsyndromic recessive deafness 5

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

Follow this condition — get notified about new trials

Broader categories

Sort by