Autosomal recessive nonsyndromic hearing loss 9

MONDO:0010986

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

Also known as: autosomal recessive nonsyndromic hearing loss 9, DFNB9, NRSD9, OTOF autosomal recessive nonsyndromic deafness, auditory neuropathy, autosomal recessive, 1, auditory neuropathy, nonsyndromic recessive, autosomal recessive deafness 9, autosomal recessive nonsyndromic deafness 9

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