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Summary Literature (0)
DOID:0080606 - anterior segment dysgenesis 1


Disease Ontology Definition:An anterior segment dysgenesis that has_material_basis_in heterozygous mutation in the PITX3 gene on chromosome 10q24.

Synonyms:

In OMIM:
OMIM:107250 - ANTERIOR SEGMENT DYSGENESIS 1; ASGD1


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

Xenbase Genes : foxe3, pax6, pitx3

Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Parent(s): autosomal dominant disease (is_a), corneal opacification and other ocular anomalies (is_a)