Click here to close Hello! We notice that you are using Internet Explorer, which is not supported by Xenbase and may cause the site to display incorrectly. We suggest using a current version of Chrome, FireFox, or Safari.
Summary Literature (0)
MIM:615887 - AMELOGENESIS IMPERFECTA, HYPOMATURATION TYPE, IIA5; AI2A5

Xenbase Genes: slc24a4

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0014385 - aryepiglottic fold
MONDO:0015048 - amelogenesis imperfecta type 2
MONDO:0019507 - amelogenesis imperfecta