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Summary Literature (0)
MIM:616270 - AMELOGENESIS IMPERFECTA, TYPE IF; AI1F

Xenbase Genes: ambn

Human Disease Resource: OMIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0014560 - amelogenesis imperfecta type 1F
MONDO:0015047 - amelogenesis imperfecta type 1
MONDO:0019507 - amelogenesis imperfecta