Amelogenesis imperfecta type 1E

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

Also known as: AIH1, AMELX amelogenesis imperfecta, amelogenesis imperfecta caused by mutation in AMELX, amelogenesis imperfecta, type 1E, X-linked dominant, AI1E, amelogenesis imperfecta X-linked 1, amelogenesis imperfecta hypoplastic/hypomaturation X-linked 1, amelogenesis imperfecta, X-linked 1

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