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Disease Ontology Browser
anterior segment dysgenesis (DOID:0060648)
Alliance: disease page
Synonyms: anterior segment developmental anomaly; corneal opacification and other ocular anomalies; sclerocornea with other ocular anomalies
Alt IDs: ICD10CM:Q13.8, OMIM:PS107250, ORDO:88632
Definition: An eye disease that is characterized by iris hypoplasia, an enlarged or reduced corneal diameter, corneal vascularization and opacity, posterior embryotoxon, corectopia, polycoria, an abnormal iridocorneal angle, ectopia lentis, and anterior synechiae between the iris and posterior corneal surface and is located_in the anterior segment of the eye.

Disease References using Mouse Models (4)

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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last database update
04/30/2024
MGI 6.23
The Jackson Laboratory