Amelogenesis imperfecta hypomaturation type 2A5

Any amelogenesis imperfecta in which the cause of the disease is a mutation in the SLC24A4 gene.

Also known as: AI2A5, SLC24A4 amelogenesis imperfecta, amelogenesis imperfecta caused by mutation in SLC24A4, amelogenesis imperfecta, type IIA5, amelogenesis imperfecta, hypomaturation type, IIA5

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