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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:
OMIM:601631 - ANTERIOR SEGMENT DYSGENESIS 3; ASGD3 |
Human Disease Resources: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Xenbase Genes

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