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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


In Mondo Disease Ontology:
MONDO:0010015 - anterior segment dysgenesis 7

Human Disease Resources: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee

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

Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Parent(s): sclerocornea (is_a)