Autosomal dominant nonsyndromic hearing loss 70

MONDO:0014853

Any autosomal dominant nonsyndromic deafness in which the cause of the disease is a mutation in the MCM2 gene.

Also known as: autosomal dominant nonsyndromic hearing loss 70, DFNA70, MCM2 autosomal dominant nonsyndromic deafness, autosomal dominant deafness 70, autosomal dominant nonsyndromic deafness 70, autosomal dominant nonsyndromic deafness caused by mutation in MCM2, autosomal dominant nonsyndromic deafness type 70, deafness, autosomal dominant 70

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