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)
DOID:0110061 - amelogenesis imperfecta hypomaturation type 2A3

Disease Ontology Definition:An amelogenesis imperfecta caused by homozygous mutation in the WDR72 gene.

Synonyms: AI2A3, amelogenesis imperfecta hypomaturation type IIA3, amelogenesis imperfecta type IIA3

Xenbase Genes : wdr72

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0013181 - amelogenesis imperfecta hypomaturation type 2A3


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

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): amelogenesis imperfecta (is_a), autosomal recessive disease (is_a)