anterior segment dysgenesis 1

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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

OMIM:107250 - ANTERIOR SEGMENT DYSGENESIS 1; ASGD1

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

Xenbase Genes Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

: 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)