Amelogenesis imperfecta type 1B

Any amelogenesis imperfecta in which the cause of the disease is a mutation in the ENAM gene.

Also known as: AI1B, ENAM amelogenesis imperfecta, amelogenesis imperfecta caused by mutation in ENAM, amelogenesis imperfecta caused by mutation in enam, enam amelogenesis imperfecta, hereditary localised enamel hypoplasia, AIH2, amelogenesis imperfecta, hypoplastic local, autosomal dominant

35 clinical trials for this condition and its sub-types.