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Summary Literature (0)
MIM:612529 - AMELOGENESIS IMPERFECTA, HYPOMATURATION TYPE, IIA2; AI2A2

Xenbase Genes: mmp20

Human Disease Resource: OMIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0012926 - amelogenesis imperfecta hypomaturation type 2A2
MONDO:0015048 - amelogenesis imperfecta type 2
MONDO:0019507 - amelogenesis imperfecta