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Autosomal dominant nonsyndromic hearing loss 22
Any autosomal dominant nonsyndromic deafness in which the cause of the disease is a mutation in the MYO6 gene. [from MONDO]
Autosomal recessive nonsyndromic hearing loss 37
Any autosomal recessive nonsyndromic deafness in which the cause of the disease is a mutation in the MYO6 gene. [from MONDO]
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