Autosomal recessive nonsyndromic hearing loss 86

MONDO:0013826

Any autosomal recessive nonsyndromic deafness in which the cause of the disease is a mutation in the TBC1D24 gene.

Also known as: DFNB86, TBC1D24 autosomal recessive nonsyndromic deafness, autosomal recessive deafness 86, autosomal recessive nonsyndromic deafness 86, autosomal recessive nonsyndromic deafness caused by mutation in TBC1D24, autosomal recessive nonsyndromic deafness type 86, deafness, autosomal recessive 86, deafness, autosomal recessive type 86

0 clinical trials for this condition and its sub-types, 0 tagged with Autosomal recessive nonsyndromic hearing loss 86 itself.

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