Amelogenesis imperfecta hypomaturation type 2A2

Any amelogenesis imperfecta in which the cause of the disease is a mutation in the MMP20 gene.

Also known as: AI2A2, MMP20 amelogenesis imperfecta, amelogenesis imperfecta caused by mutation in MMP20, amelogenesis imperfecta, type IIA2, amelogenesis imperfecta, hypomaturation type, IIA2, amelogenesis imperfecta, pigmented hypomaturation type, 2

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