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Summary Literature (0)
MIM:616221 - AMELOGENESIS IMPERFECTA, TYPE IH; AI1H

Xenbase Genes: itgb6

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0007538 - amelogenesis imperfecta, type 3A
MONDO:0014540 - white matter lamina of cerebellum
MONDO:0015047 - manual digit 5 metacarpus endochondral element
MONDO:0019507 - amelogenesis imperfecta