Additional Disease Briefs

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Rare Disease Database Reports Additional Rare Disease Briefs
autosomal recessive nonsyndromic hearing loss 15

Also known as: DFNB15, DFNB72, DFNB95, GIPC3 autosomal recessive nonsyndromic deafness, autosomal recessive deafness 15, autosomal recessive deafness 72, autosomal recessive deafness 95, autosomal recessive nonsyndromic deafness 15, autosomal recessive nonsyndromic deafness caused by mutation in GIPC3, autosomal recessive nonsyndromic deafness type 15, autosomal recessive nonsyndromic hearing loss 15, deafness, autosomal recessive 15, deafness, autosomal recessive 72, deafness, autosomal recessive 95, deafness, autosomal recessive type 15

autosomal recessive nonsyndromic hearing loss 16

Also known as: DFNB16, STRC autosomal recessive nonsyndromic deafness, autosomal recessive deafness 16, autosomal recessive nonsyndromic deafness 16, autosomal recessive nonsyndromic deafness caused by mutation in STRC, autosomal recessive nonsyndromic deafness type 16, autosomal recessive nonsyndromic hearing loss 16, deafness, autosomal recessive 16, deafness, autosomal recessive type 16

autosomal recessive nonsyndromic hearing loss 18A

Also known as: DFNB18A, USH1C autosomal recessive nonsyndromic deafness, autosomal recessive deafness 18A, autosomal recessive nonsyndromic deafness 18A, autosomal recessive nonsyndromic deafness caused by mutation in USH1C, autosomal recessive nonsyndromic deafness type 18A, deafness, autosomal recessive 18, deafness, autosomal recessive 18A, deafness, autosomal recessive 18a, deafness, autosomal recessive type 18A

autosomal recessive nonsyndromic hearing loss 18B

Also known as: DFNB18B, OTOG autosomal recessive nonsyndromic deafness, autosomal recessive deafness 18B, autosomal recessive nonsyndromic deafness 18B, autosomal recessive nonsyndromic deafness caused by mutation in OTOG, autosomal recessive nonsyndromic deafness type 18B, autosomal recessive nonsyndromic hearing loss 18B, deafness, autosomal recessive 18B, deafness, autosomal recessive 18b, deafness, autosomal recessive type 18B

autosomal recessive nonsyndromic hearing loss 1A

Also known as: DFNB1, DFNB1A, GJB2-related deafness, autosomal recessive deafness 1A, autosomal recessive nonsyndromic deafness 1A, autosomal recessive nonsyndromic deafness type 1A, autosomal recessive nonsyndromic hearing loss 1A, connexin 26 deafness, deafness nonsyndromic, connexin 26 linked, deafness, autosomal recessive 1A, deafness, autosomal recessive 1a, autosomal recessive, digenic dominant, deafness, autosomal recessive type 1A, deafness, digenic GJB2/GJB6, Autosomal recessive, Digenic dominant, deafness, digenic, GJB2/GJB3, deafness, digenic, GJB2/GJB3, Autosomal recessive, Digenic dominant, deafness, digenic, GJB2/GJB6

autosomal recessive nonsyndromic hearing loss 1B

Also known as: Autosomal recessive deafness type 1B, DFNB1B, GJB6 autosomal recessive nonsyndromic deafness, autosomal recessive deafness 1B, autosomal recessive nonsyndromic deafness 1B, autosomal recessive nonsyndromic deafness caused by mutation in GJB6, autosomal recessive nonsyndromic deafness type 1B, deafness, autosomal recessive 1B, deafness, autosomal recessive 1b, deafness, autosomal recessive type 1B

autosomal recessive nonsyndromic hearing loss 2

Also known as: DFNB2, MYO7A autosomal recessive nonsyndromic deafness, autosomal recessive deafness 2, autosomal recessive nonsyndromic deafness 2, autosomal recessive nonsyndromic deafness caused by mutation in MYO7A, autosomal recessive nonsyndromic deafness type 2, deafness, autosomal recessive 2, deafness, autosomal recessive type 2, neurosensory nonsyndromic recessive deafness 2

autosomal recessive nonsyndromic hearing loss 21

Also known as: DFNB21, TECTA autosomal recessive nonsyndromic deafness, autosomal recessive deafness 21, autosomal recessive nonsyndromic deafness 21, autosomal recessive nonsyndromic deafness caused by mutation in TECTA, autosomal recessive nonsyndromic deafness caused by mutation in tecta, autosomal recessive nonsyndromic deafness type 21, autosomal recessive nonsyndromic hearing loss 21, deafness, autosomal recessive 21, deafness, autosomal recessive type 21, tecta autosomal recessive nonsyndromic deafness

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