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

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