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Summary Literature (0)
DOID:0060648 - anterior segment dysgenesis

Disease Ontology Definition:An eye disease that is characterized by iris hypoplasia, an enlarged or reduced corneal diameter, corneal vascularization and opacity, posterior embryotoxon, corectopia, polycoria, an abnormal iridocorneal angle, ectopia lentis, and anterior synechiae between the iris and posterior corneal surface and is located_in the anterior segment of the eye.

Synonyms: anterior segment developmental anomaly, corneal opacification and other ocular anomalies, sclerocornea with other ocular anomalies

Xenbase Genes : foxc1, foxe3, pitx2, pax6, pitx3, pxdn, cyp1b1, cpamd8, atoh7

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0010015 - anterior segment dysgenesis 7


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

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): eye disease (is_a), monogenic disease (is_a), sclerocornea (is_a)