Autosomal dominant nonsyndromic hearing loss 1

MONDO:0007424

Any autosomal dominant nonsyndromic deafness in which the cause of the disease is a mutation in the DIAPH1 gene.

Also known as: Konigsmark syndrome, DFNA1, DIAPH1 autosomal dominant nonsyndromic deafness, autosomal dominant deafness 1, autosomal dominant nonsyndromic deafness 1, autosomal dominant nonsyndromic deafness caused by mutation in DIAPH1, autosomal dominant nonsyndromic deafness type 1, deafness, autosomal dominant 1

0 clinical trials for this condition and its sub-types, 0 tagged with Autosomal dominant nonsyndromic hearing loss 1 itself.

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Including sub-types (0) Tagged with Autosomal dominant nonsyndromic hearing loss 1 (0)

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