anterior segment dysgenesis 3

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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

OMIM:601631 - ANTERIOR SEGMENT DYSGENESIS 3; ASGD3

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

: 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)