Any amelogenesis imperfecta in which the cause of the disease is a mutation in the DLX3 gene.
Comprehensive, easy-to-understand information about this condition
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amelogenesis imperfecta type 1G
MONDO:0008771
X-linked amelogenesis imperfecta hypoplastic/hypomaturation 2
MONDO:0010522
amelogenesis imperfecta type 1
MONDO:0015047
amelogenesis imperfecta type 2
MONDO:0015048
amelogenesis imperfecta, IIa 1K
MONDO:0031084
hypocalcified amelogenesis imperfecta
MONDO:0968955