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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:
OMIM:107250 - ANTERIOR SEGMENT DYSGENESIS 1; ASGD1 |
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)