Additional Disease Briefs

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Rare Disease Database Reports Additional Rare Disease Briefs
autosomal dominant nonsyndromic hearing loss 25

Also known as: DFNA25, SLC17A8 autosomal dominant nonsyndromic deafness, autosomal dominant deafness 25, autosomal dominant nonsyndromic deafness 25, autosomal dominant nonsyndromic deafness caused by mutation in SLC17A8, autosomal dominant nonsyndromic deafness type 25, deafness, autosomal dominant 25, deafness, autosomal dominant type 25

autosomal dominant nonsyndromic hearing loss 28

Also known as: DFNA28, GRHL2 autosomal dominant nonsyndromic deafness, autosomal dominant deafness 28, autosomal dominant nonsyndromic deafness 28, autosomal dominant nonsyndromic deafness caused by mutation in GRHL2, autosomal dominant nonsyndromic deafness type 28, deafness, autosomal dominant 28, deafness, autosomal dominant type 28

autosomal dominant nonsyndromic hearing loss 2A

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, deafness, autosomal dominant type 2A

autosomal dominant nonsyndromic hearing loss 2B

Also known as: DFNA2B, GJB3 autosomal dominant nonsyndromic deafness, autosomal dominant deafness 2B, autosomal dominant nonsyndromic deafness 2B, autosomal dominant nonsyndromic deafness caused by mutation in GJB3, autosomal dominant nonsyndromic deafness type 2B, deafness, autosomal dominant 2B, deafness, autosomal dominant 2b, deafness, autosomal dominant type 2B

autosomal dominant nonsyndromic hearing loss 36

Also known as: DFNA36, TMC1 autosomal dominant nonsyndromic deafness, autosomal dominant deafness 36, autosomal dominant nonsyndromic deafness 36, autosomal dominant nonsyndromic deafness caused by mutation in TMC1, autosomal dominant nonsyndromic deafness type 36, deafness, autosomal dominant 36, deafness, autosomal dominant type 36

autosomal dominant nonsyndromic hearing loss 3A

Also known as: DFNA3, DFNA3A, GJB2 autosomal dominant nonsyndromic deafness, NSRD1, autosomal dominant deafness 3A, autosomal dominant nonsyndromic deafness 3A, autosomal dominant nonsyndromic deafness caused by mutation in GJB2, autosomal dominant nonsyndromic deafness type 3A, deafness, autosomal dominant 3A, deafness, autosomal dominant 3a, deafness, autosomal dominant nonsyndromic sensorineural 3, deafness, autosomal dominant type 3A, neurosensory nonsyndromic dominant deafness 1

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