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Amelogenesis imperfecta type 1E

MONDO:0010521

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

Also known as: AIH1, AMELX amelogenesis imperfecta, amelogenesis imperfecta caused by mutation in AMELX, amelogenesis imperfecta, type 1E, X-linked dominant, AI1E, amelogenesis imperfecta X-linked 1, amelogenesis imperfecta hypoplastic/hypomaturation X-linked 1, amelogenesis imperfecta, X-linked 1

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

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