Autosomal dominant nonsyndromic hearing loss 17

MONDO:0011350

Any autosomal dominant nonsyndromic deafness in which the cause of the disease is a mutation in the MYH9 gene.

Also known as: DFNA17, MYH9 autosomal dominant nonsyndromic deafness, autosomal dominant deafness 17, autosomal dominant nonsyndromic deafness 17, autosomal dominant nonsyndromic deafness caused by mutation in MYH9, autosomal dominant nonsyndromic deafness type 17, deafness, autosomal dominant 17, deafness, autosomal dominant nonsyndromic sensorineural 17

60 clinical trials for this condition and its sub-types.

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