Amelogenesis imperfecta hypomaturation type 2A3

Any amelogenesis imperfecta in which the cause of the disease is a mutation in the WDR72 gene.

Also known as: AI2A3, WDR72 amelogenesis imperfecta, amelogenesis imperfecta caused by mutation in WDR72, amelogenesis imperfecta hypomaturation type 2A3, amelogenesis imperfecta, type IIA3, amelogenesis imperfecta, hypomaturation type, IIA3

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