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Results 1 - 4 of 4 for "Deafness," autosomal dominant 44
  1. ACTG1 gene 
    ... gamma 1 actin-like protein cytoskeletal gamma-actin deafness, autosomal dominant 20 deafness, autosomal dominant 26 DFNA20 DFNA26 gamma-actin Tests of ACTG1 ...
    https://medlineplus.gov/genetics/gene/actg1 - Genetics
  2. TBC1D24 gene 
    ... Black-Ziegelbein EA, Smith RJ. TBC1D24 mutation causes autosomal-dominant nonsyndromic hearing loss. Hum Mutat. 2014 Jul;35( ... a gene associated with epilepsy, also cause nonsyndromic deafness DFNB86. Am J Hum ... T, Wu H. A dominant mutation in the stereocilia-expressing gene TBC1D24 is ...
    https://medlineplus.gov/genetics/gene/tbc1d24 - Genetics
  3. Noonan syndrome with multiple lentigines 
    ... syndrome with multiple lentigines is inherited in an autosomal dominant pattern, which means one copy of the altered ...
    https://medlineplus.gov/.../noonan-syndrome-with-multiple-lentigines - Genetics
  4. Lacrimo-auriculo-dento-digital syndrome 
    ... FGFR2 FGFR3 This condition is inherited in an autosomal dominant pattern, which means a mutation in one copy ...
    https://medlineplus.gov/.../lacrimo-auriculo-dento-digital-syndrome - Genetics