autosomal dominant nonsyndromic hearing loss 16
Also known as: DFNA16, autosomal dominant deafness 16, autosomal dominant nonsyndromic deafness 16, autosomal dominant nonsyndromic deafness type 16, deafness, autosomal dominant 16
Also known as: DFNA16, autosomal dominant deafness 16, autosomal dominant nonsyndromic deafness 16, autosomal dominant nonsyndromic deafness type 16, deafness, autosomal dominant 16
Also known as: DFNA17, MYH9 autosomal dominant nonsyndromic deafness, autosomal dominant deafness 17, autosomal dominant nonsyndromic deafness 17, autosomal dominant nonsyndromic deafness caused by mutation in MYH9, autosomal dominant nonsyndromic deafness type 17, cochleosaccular degeneration, deafness, autosomal dominant 17, deafness, autosomal dominant nonsyndromic sensorineural 17, deafness, autosomal dominant type 17, late-onset progressive hereditary hearing impairment due to cochleosaccular degeneration, nonsyndromic hereditary deafness DFNA17
Also known as: DFNA18, autosomal dominant deafness 18, autosomal dominant nonsyndromic deafness 18, autosomal dominant nonsyndromic deafness type 18, deafness, autosomal dominant 18
Also known as: ACTG1 autosomal dominant nonsyndromic deafness, DFNA20, DFNA26, autosomal dominant deafness 20, autosomal dominant nonsyndromic deafness 20, autosomal dominant nonsyndromic deafness caused by mutation in ACTG1, autosomal dominant nonsyndromic deafness type 20, deafness, autosomal dominant 20, deafness, autosomal dominant 20/26, deafness, autosomal dominant type 20
Also known as: DFNA21, autosomal dominant deafness 21, autosomal dominant nonsyndromic deafness 21, autosomal dominant nonsyndromic deafness type 21, deafness, autosomal dominant 21
Also known as: DFNA 22, DFNA22, MYO6 autosomal dominant nonsyndromic deafness, autosomal dominant deafness 22, autosomal dominant nonsyndromic deafness 22, autosomal dominant nonsyndromic deafness caused by mutation in MYO6, autosomal dominant nonsyndromic deafness type 22, deafness, autosomal dominant 22, deafness, autosomal dominant 22, with hypertrophic cardiomyopathy, deafness, autosomal dominant nonsyndromic sensorineural 22, deafness, autosomal dominant type 22
Also known as: DFNA 23, DFNA23, SIX1 autosomal dominant nonsyndromic deafness, autosomal dominant deafness 23, autosomal dominant nonsyndromic deafness 23, autosomal dominant nonsyndromic deafness caused by mutation in SIX1, autosomal dominant nonsyndromic deafness type 23, deafness, autosomal dominant 23, deafness, autosomal dominant nonsyndromic sensorineural 23, deafness, autosomal dominant type 23
Also known as: DFNA 24, DFNA24, autosomal dominant deafness 24, autosomal dominant nonsyndromic deafness 24, autosomal dominant nonsyndromic deafness type 24, deafness, autosomal dominant 24, deafness, autosomal dominant nonsyndromic sensorineural 24
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
Also known as: DFNA27, autosomal dominant deafness 27, autosomal dominant nonsyndromic deafness 27, autosomal dominant nonsyndromic deafness type 27, deafness, autosomal dominant 27