Amelogenesis imperfecta type 2A1

Any amelogenesis imperfecta in which the cause of the disease is a mutation in the KLK4 gene.

Also known as: AI2A1, KLK4 amelogenesis imperfecta, amelogenesis imperfecta caused by mutation in KLK4, amelogenesis imperfecta, type IIA1, amelogenesis imperfecta pigmented hypomaturation type, amelogenesis imperfecta, hypomaturation type, IIA1, amelogenesis imperfecta, pigmented hypomaturation type, 1

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