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:0060648 - corneal opacification and other ocular anomalies

Disease Ontology Definition:A sclerocornea that has_material_basis_in homozygous or compound heterozygous mutation in the PXDN gene on chromosome 2p25 and is characterized by corneal opacifiaction, cataract, microcornea, microphthalmia, and anterior segment dysgenesis.

Synonyms: 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: AGR, MGI, ZFIN, FlyBase, WormBase, RGD

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