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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,
Echinobase Genes : pax6, foxc1
Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s):
sclerocornea (is_a)