Autosomal recessive nonsyndromic hearing loss 91

MONDO:0013269

Any autosomal recessive nonsyndromic deafness in which the cause of the disease is a mutation in the SERPINB6 gene.

Also known as: autosomal recessive nonsyndromic hearing loss 91, DFNB91, SERPINB6 autosomal recessive nonsyndromic deafness, autosomal recessive deafness 91, autosomal recessive nonsyndromic deafness 91, autosomal recessive nonsyndromic deafness caused by mutation in SERPINB6, autosomal recessive nonsyndromic deafness type 91, deafness, autosomal recessive 91

0 clinical trials for this condition and its sub-types, 0 tagged with Autosomal recessive nonsyndromic hearing loss 91 itself.

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↑ Hearing loss, autosomal recessive (17)

Including sub-types (0) Tagged with Autosomal recessive nonsyndromic hearing loss 91 (0)

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