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Summary Literature (0)
DOID:0080608 - anterior segment dysgenesis 3


Disease Ontology Definition:An anterior segment dysgenesis that has_material_basis_in heterozygous mutation in the FOXC1 gene on chromosome 6p25.

Synonyms:

In OMIM:
OMIM:601631 - ANTERIOR SEGMENT DYSGENESIS 3; ASGD3


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

Xenbase Genes : foxc1

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