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Summary Literature (0)
MIM:613211 - AMELOGENESIS IMPERFECTA, HYPOMATURATION TYPE, IIA3; AI2A3

Xenbase Genes: wdr72

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0013181 - amelogenesis imperfecta hypomaturation type 2A3
MONDO:0015048 - amelogenesis imperfecta type 2
MONDO:0019507 - amelogenesis imperfecta

Disease Ontology (DO):
DOID:0110061 - amelogenesis imperfecta hypomaturation type 2A3