Additional Disease Briefs

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Rare Disease Database Reports Additional Rare Disease Briefs
autosomal dominant nonsyndromic hearing loss 3B

Also known as: DFNA3B, GJB6 autosomal dominant nonsyndromic deafness, autosomal dominant deafness 3B, autosomal dominant nonsyndromic deafness 3B, autosomal dominant nonsyndromic deafness caused by mutation in GJB6, autosomal dominant nonsyndromic deafness type 3B, deafness, autosomal dominant 3B, deafness, autosomal dominant 3b, deafness, autosomal dominant type 3B

autosomal dominant nonsyndromic hearing loss 40

Also known as: CRYM autosomal dominant nonsyndromic deafness, DFNA40, autosomal dominant deafness 40, autosomal dominant nonsyndromic deafness 40, autosomal dominant nonsyndromic deafness caused by mutation in CRYM, autosomal dominant nonsyndromic deafness type 40, autosomal dominant nonsyndromic hearing loss 40, deafness, autosomal dominant 40, deafness, autosomal dominant type 40

autosomal dominant nonsyndromic hearing loss 41

Also known as: DFNA41, P2RX2 autosomal dominant nonsyndromic deafness, autosomal dominant deafness 41, autosomal dominant nonsyndromic deafness 41, autosomal dominant nonsyndromic deafness caused by mutation in P2RX2, autosomal dominant nonsyndromic deafness type 41, deafness, autosomal dominant 41, deafness, autosomal dominant type 41

autosomal dominant nonsyndromic hearing loss 44

Also known as: CCDC50 autosomal dominant nonsyndromic deafness, DFNA44, autosomal dominant deafness 44, autosomal dominant nonsyndromic deafness 44, autosomal dominant nonsyndromic deafness caused by mutation in CCDC50, autosomal dominant nonsyndromic deafness type 44, deafness, autosomal dominant 44, deafness, autosomal dominant type 44

autosomal dominant nonsyndromic hearing loss 48

Also known as: DFNA48, MYO1A autosomal dominant nonsyndromic deafness, autosomal dominant deafness 48, autosomal dominant nonsyndromic deafness 48, autosomal dominant nonsyndromic deafness caused by mutation in MYO1A, autosomal dominant nonsyndromic deafness type 48, deafness, autosomal dominant 48, deafness, autosomal dominant type 48

autosomal dominant nonsyndromic hearing loss 4A

Also known as: DFNA4A, MYH14 autosomal dominant nonsyndromic deafness, autosomal dominant deafness 4A, autosomal dominant nonsyndromic deafness 4A, autosomal dominant nonsyndromic deafness caused by mutation in MYH14, autosomal dominant nonsyndromic deafness type 4A, deafness, autosomal dominant 4, deafness, autosomal dominant 4A, deafness, autosomal dominant 4a, deafness, autosomal dominant type 4A

autosomal dominant nonsyndromic hearing loss 4B

Also known as: CEACAM16 autosomal dominant nonsyndromic deafness, DFNA4B, autosomal dominant deafness 4B, autosomal dominant nonsyndromic deafness 4B, autosomal dominant nonsyndromic deafness caused by mutation in CEACAM16, autosomal dominant nonsyndromic deafness type 4B, deafness, autosomal dominant 4B, deafness, autosomal dominant 4b, deafness, autosomal dominant type 4B

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