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Summary Literature (0)
DOID:2187 - amelogenesis imperfecta

Disease Ontology Definition:A dental enamel hypoplasia characterized by abnormal enamel formation.

Synonyms:

Xenbase Genes : slc24a4, amelx, mmp20, ambn, itgb6, lamb3, wdr72, fam83h, dlx3, fam20a, enam, fam20a.2

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0019507 - amelogenesis imperfecta


Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): dental enamel hypoplasia (is_a)