Autosomal recessive nonsyndromic hearing loss 36

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

Also known as: autosomal recessive nonsyndromic hearing loss 36, deafness, neurosensory, without vestibular involvement, autosomal dominant, DFNB36, ESPN autosomal recessive nonsyndromic deafness, autosomal recessive deafness 36, autosomal recessive nonsyndromic deafness 36, autosomal recessive nonsyndromic deafness caused by mutation in ESPN, autosomal recessive nonsyndromic deafness type 36

0 clinical trials for this condition and its sub-types, 0 tagged with Autosomal recessive nonsyndromic hearing loss 36 itself.