Additional Disease Briefs

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Rare Disease Database Reports Additional Rare Disease Briefs
autosomal dominant nonsyndromic hearing loss 13

Also known as: COL11A2 autosomal dominant nonsyndromic deafness, DFNA13, autosomal dominant deafness 13, autosomal dominant nonsyndromic deafness 13, autosomal dominant nonsyndromic deafness caused by mutation in COL11A2, autosomal dominant nonsyndromic deafness type 13, deafness, autosomal dominant 13, deafness, autosomal dominant type 13

autosomal dominant nonsyndromic hearing loss 15

Also known as: DFNA15, POU4F3 autosomal dominant nonsyndromic deafness, autosomal dominant deafness 15, autosomal dominant nonsyndromic deafness 15, autosomal dominant nonsyndromic deafness caused by mutation in POU4F3, autosomal dominant nonsyndromic deafness type 15, deafness, autosomal dominant 15, deafness, autosomal dominant type 15

autosomal dominant nonsyndromic hearing loss 17

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

autosomal dominant nonsyndromic hearing loss 20

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

autosomal dominant nonsyndromic hearing loss 22

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

autosomal dominant nonsyndromic hearing loss 23

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

autosomal dominant nonsyndromic hearing loss 24

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

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