Additional Disease Briefs

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Rare Disease Database Reports Additional Rare Disease Briefs
autosomal dominant nonsyndromic hearing loss 5

Also known as: DFNA5, GSDME autosomal dominant nonsyndromic deafness, autosomal dominant deafness 5, autosomal dominant nonsyndromic deafness 5, autosomal dominant nonsyndromic deafness caused by mutation in GSDME, autosomal dominant nonsyndromic deafness type 5, deafness, autosomal dominant 5, deafness, autosomal dominant type 5

autosomal dominant nonsyndromic hearing loss 50

Also known as: DFNA50, autosomal dominant deafness 50, autosomal dominant nonsyndromic deafness 50, autosomal dominant nonsyndromic deafness type 50, deafness, autosomal dominant 50, deafness, autosomal dominant type 50

autosomal dominant nonsyndromic hearing loss 51

Also known as: DFNA51, autosomal dominant deafness 51, autosomal dominant nonsyndromic deafness 51, autosomal dominant nonsyndromic deafness type 51, chromosome 9Q21.11 Duplication syndrome, chromosome 9q21.11 duplication syndrome, deafness, autosomal dominant 51, deafness, autosomal dominant type 51

autosomal dominant nonsyndromic hearing loss 52

Also known as: DFNA52, autosomal dominant deafness 52, autosomal dominant nonsyndromic deafness 52, autosomal dominant nonsyndromic deafness type 52, deafness, autosomal dominant 42, deafness, autosomal dominant 52

autosomal dominant nonsyndromic hearing loss 53

Also known as: DFNA53, autosomal dominant deafness 53, autosomal dominant nonsyndromic deafness 53, autosomal dominant nonsyndromic deafness type 53, deafness, autosomal dominant 53, deafness, autosomal dominant nonsyndromic sensorineural 53

autosomal dominant nonsyndromic hearing loss 56

Also known as: DFNA56, TNC autosomal dominant nonsyndromic deafness, autosomal dominant deafness 56, autosomal dominant nonsyndromic deafness 56, autosomal dominant nonsyndromic deafness caused by mutation in TNC, autosomal dominant nonsyndromic deafness type 56, deafness, autosomal dominant 56, deafness, autosomal dominant type 56

autosomal dominant nonsyndromic hearing loss 6

Also known as: DFNA14, DFNA38, DFNA6, WFS1 autosomal dominant nonsyndromic deafness, autosomal dominant deafness 14, autosomal dominant deafness 38, autosomal dominant deafness 6, autosomal dominant nonsyndromic deafness 6, autosomal dominant nonsyndromic deafness caused by mutation in WFS1, autosomal dominant nonsyndromic deafness type 6, deafness, autosomal dominant 14, deafness, autosomal dominant 38, deafness, autosomal dominant 6, deafness, autosomal dominant 6/14/38, deafness, autosomal dominant type 6

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