(Q27674800)

English

amelogenesis imperfecta type 3

amelogenesis imperfecta that has material basis in heterozygous mutation in the FAM83H gene

  • ADHCAI
  • AI3
  • amelogenesis imperfecta hypomineralization type
  • amelogenesis imperfecta type III
  • autosomal dominant amelogenesis imperfecta hypocalcification type
  • amelogenesis imperfecta type 3A

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