Autosomal recessive nonsyndromic hearing loss 46

MONDO:0012327

An autosomal recessive nonsyndromic deafness that has material basis in variation in the chromosome region 18p11.32-p11.31.

Also known as: DFNB46, autosomal recessive deafness 46, autosomal recessive nonsyndromic deafness 46, autosomal recessive nonsyndromic deafness type 46, deafness, autosomal recessive 46

0 clinical trials for this condition and its sub-types, 0 tagged with Autosomal recessive nonsyndromic hearing loss 46 itself.

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↑ Hearing loss, autosomal recessive (17)

Including sub-types (0) Tagged with Autosomal recessive nonsyndromic hearing loss 46 (0)

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