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Disease Ontology Browser
anterior segment dysgenesis 2 (DOID:0080607)
Alliance: disease page
Synonyms: ASGD2; congenital absence of lens; congenital aphakia; congenital primary aphakia; CPAK
Alt IDs: OMIM:610256, ICD10CM:Q12.3, NCI:C222344, UMLS_CUI:C0152422
Definition: An anterior segment dysgenesis that has_material_basis_in homozygous, compound heterozygous, or heterozygous mutation in the FOXE3 gene on chromosome 1p33.

Disease References using Mouse Models (2)
Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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Send questions and comments to User Support. 		last database update
09/08/2026
MGI 6.24 		The Jackson Laboratory