|
DOID:2187 - amelogenesis imperfecta
Disease Ontology Definition:A dental enamel hypoplasia characterized by abnormal enamel formation.
Synonyms:
Xenbase Genes
![Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries](img/icons/info1.png)
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)