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Summary Literature (0)
MIM:204690 - AMELOGENESIS IMPERFECTA, TYPE IG; AI1G

Xenbase Genes: fam20a, fam20a.2

Human Disease Resource: OMIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0008771 - amelogenesis imperfecta type 1G

Disease Ontology (DO):
DOID:0110066 - amelogenesis imperfecta type 1G