Additional Disease Briefs
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
Also known as:
DFNA64, DIABLO autosomal dominant nonsyndromic deafness, autosomal dominant deafness 64, autosomal dominant nonsyndromic deafness 64, autosomal dominant nonsyndromic deafness caused by mutation in DIABLO, autosomal dominant nonsyndromic deafness type 64, deafness, autosomal dominant 64, deafness, autosomal dominant type 64
Also known as:
DFNA65, TBC1D24 autosomal dominant nonsyndromic deafness, autosomal dominant deafness 65, autosomal dominant nonsyndromic deafness 65, autosomal dominant nonsyndromic deafness caused by mutation in TBC1D24, autosomal dominant nonsyndromic deafness type 65, deafness, autosomal dominant 65, deafness, autosomal dominant type 65
Also known as:
CD164 autosomal dominant nonsyndromic deafness, DFNA66, autosomal dominant deafness 66, autosomal dominant nonsyndromic deafness 66, autosomal dominant nonsyndromic deafness caused by mutation in CD164, autosomal dominant nonsyndromic deafness type 66, deafness, autosomal dominant 66, deafness, autosomal dominant type 66
Also known as:
DFNA67, OSBPL2 autosomal dominant nonsyndromic deafness, autosomal dominant deafness 67, autosomal dominant nonsyndromic deafness 67, autosomal dominant nonsyndromic deafness caused by mutation in OSBPL2, autosomal dominant nonsyndromic deafness type 67, deafness, autosomal dominant 67, deafness, autosomal dominant type 67
Also known as:
DFNA68, HOMER2 autosomal dominant nonsyndromic deafness, autosomal dominant deafness 68, autosomal dominant nonsyndromic deafness 68, autosomal dominant nonsyndromic deafness caused by mutation in HOMER2, autosomal dominant nonsyndromic deafness type 68, deafness, autosomal dominant 68, deafness, autosomal dominant type 68
Also known as:
DCUA, DFNA69, KITLG autosomal dominant nonsyndromic deafness, autosomal dominant deafness 69, autosomal dominant nonsyndromic deafness 69, autosomal dominant nonsyndromic deafness caused by mutation in KITLG, autosomal dominant nonsyndromic deafness type 69, deafness, autosomal dominant 69, deafness, autosomal dominant 69, unilateral or asymmetric, deafness, congenital, unilateral or asymmetric, unilateral or asymmetric congenital deafness
Also known as:
DFNA7, autosomal dominant deafness 7, autosomal dominant nonsyndromic deafness 7, autosomal dominant nonsyndromic deafness type 7, deafness, autosomal dominant 7
Also known as:
DFNA70, MCM2 autosomal dominant nonsyndromic deafness, autosomal dominant deafness 70, autosomal dominant nonsyndromic deafness 70, autosomal dominant nonsyndromic deafness caused by mutation in MCM2, autosomal dominant nonsyndromic deafness type 70, autosomal dominant nonsyndromic hearing loss 70, deafness, autosomal dominant 70, deafness, autosomal dominant type 70
Also known as:
COCH autosomal dominant nonsyndromic deafness, DFNA9, autosomal dominant deafness 9, autosomal dominant nonsyndromic deafness 9, autosomal dominant nonsyndromic deafness caused by mutation in COCH, autosomal dominant nonsyndromic deafness type 9, deafness, autosomal dominant 9, deafness, autosomal dominant type 9
