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Summary Literature (0)
MIM:617217 - AMELOGENESIS IMPERFECTA, HYPOMATURATION TYPE, IIA6; AI2A6

Xenbase Genes: gpr68

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0014971 - amelogenesis imperfecta, hypomaturation type, IIa6
MONDO:0015048 - amelogenesis imperfecta type 2
MONDO:0019507 - amelogenesis imperfecta