Autosomal recessive nonsyndromic hearing loss 23

MONDO:0012293

Any autosomal recessive nonsyndromic deafness in which the cause of the disease is a mutation in the PCDH15 gene.

Also known as: DFNB23, PCDH15 autosomal recessive nonsyndromic deafness, autosomal recessive deafness 23, autosomal recessive nonsyndromic deafness 23, autosomal recessive nonsyndromic deafness caused by mutation in PCDH15, autosomal recessive nonsyndromic deafness type 23, deafness, autosomal recessive 23, deafness, autosomal recessive type 23

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