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Autosomal dominant nonsyndromic hearing loss 68

MONDO:0014740

Any autosomal dominant nonsyndromic deafness in which the cause of the disease is a mutation in the HOMER2 gene.

Also known as: DFNA68, HOMER2 autosomal dominant nonsyndromic deafness, autosomal dominant deafness 68, autosomal dominant nonsyndromic deafness 68, autosomal dominant nonsyndromic deafness caused by mutation in HOMER2, autosomal dominant nonsyndromic deafness type 68, deafness, autosomal dominant 68, deafness, autosomal dominant type 68

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