Amelogenesis imperfecta hypomaturation type 2A3
MONDO:0013181Any 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
1 clinical trial for this condition and its sub-types.
Follow this condition — get notified about new trials