Autosomal recessive nonsyndromic hearing loss 20

MONDO:0011392

An autosomal recessive nonsyndromic deafness that has material basis in variation in the chromosome region 11q25-qter.

Also known as: DFNB20, autosomal recessive deafness 20, autosomal recessive nonsyndromic deafness 20, autosomal recessive nonsyndromic deafness type 20, deafness, autosomal recessive 20

0 clinical trials for this condition and its sub-types, 0 tagged with Autosomal recessive nonsyndromic hearing loss 20 itself.

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↑ Hearing loss, autosomal recessive (17)

Including sub-types (0) Tagged with Autosomal recessive nonsyndromic hearing loss 20 (0)

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