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Summary Literature (0)
DOID:0080607 - anterior segment dysgenesis 2

Disease Ontology Definition:An anterior segment dysgenesis that has_material_basis_in homozygous, compound heterozygous, or heterozygous mutation in the FOXE3 gene on chromosome 1p33.

Synonyms:

Xenbase Genes : foxe3


MIM:
MIM:610256 - ANTERIOR SEGMENT DYSGENESIS 2; ASGD2

Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): anterior segment dysgenesis (is_a), autosomal recessive disease (is_a)