Autosomal dominant nonsyndromic hearing loss 2A

MONDO:0010817

Any autosomal dominant nonsyndromic deafness in which the cause of the disease is a mutation in the KCNQ4 gene.

Also known as: DFNA2A, KCNQ4 autosomal dominant nonsyndromic deafness, autosomal dominant deafness 2A, autosomal dominant nonsyndromic deafness 2A, autosomal dominant nonsyndromic deafness caused by mutation in KCNQ4, autosomal dominant nonsyndromic deafness type 2A, deafness, autosomal dominant 2A, deafness, autosomal dominant 2a

0 clinical trials for this condition and its sub-types, 0 tagged with Autosomal dominant nonsyndromic hearing loss 2A itself.

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