Amelogenesis imperfecta hypomaturation type 2A3

MONDO:0013181

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

1 clinical trial for this condition and its sub-types, 0 tagged with Amelogenesis imperfecta hypomaturation type 2A3 itself.

Follow this condition to get notified about new trials

Where it sits in the disease tree

Browse by category →

Part of

↑ Amelogenesis imperfecta type 2 (0)

Including sub-types (1) Tagged with Amelogenesis imperfecta hypomaturation type 2A3 (0)

We haven't found any trials for this condition yet. Follow it to get notified when new trials appear.