Amelogenesis imperfecta, type 3A

Any amelogenesis imperfecta in which the cause of the disease is a mutation in the FAM83H gene.

Also known as: amelogenesis imperfecta hypomineralization type, amelogenesis imperfecta type 3, amelogenesis imperfecta type III, ADHCAI, AI3, FAM83H amelogenesis imperfecta, amelogenesis imperfecta caused by mutation in FAM83H, amelogenesis imperfecta, type 3A

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