Autosomal recessive nonsyndromic hearing loss 96

MONDO:0013738

An autosomal recessive nonsyndromic deafness that has material basis in variation in the chromosome region 1p36.31-p36.13.

Also known as: DFNB96, autosomal recessive deafness 96, autosomal recessive nonsyndromic deafness 96, autosomal recessive nonsyndromic deafness type 96, deafness, autosomal recessive 96

0 clinical trials for this condition and its sub-types, 0 tagged with Autosomal recessive nonsyndromic hearing loss 96 itself.

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↑ Hearing loss, autosomal recessive (17)

Including sub-types (0) Tagged with Autosomal recessive nonsyndromic hearing loss 96 (0)

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