Autosomal recessive nonsyndromic hearing loss 88

Any autosomal recessive nonsyndromic deafness in which the cause of the disease is a mutation in the ELMOD3 gene.

Also known as: DFNB88, ELMOD3 autosomal recessive nonsyndromic deafness, autosomal recessive deafness 88, autosomal recessive nonsyndromic deafness 88, autosomal recessive nonsyndromic deafness caused by mutation in ELMOD3, autosomal recessive nonsyndromic deafness type 88, deafness, autosomal recessive 88, deafness, autosomal recessive type 88

0 clinical trials for this condition and its sub-types, 0 tagged with Autosomal recessive nonsyndromic hearing loss 88 itself.