FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
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General Information
Term anterior segment dysgenesis ID (Ontology) DOID:0060648 (Human Disease)
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.
Also Known As "anterior segment developmental anomaly" ; "corneal opacification and other ocular anomalies" ; "sclerocornea with other ocular anomalies"
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Spanning Tree (Parents/Children)
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sensory system disease
 |__eye disease________
genetic disease        |
 |__monogenic disease__|
                       anterior segment dysgenesis  19 rec.
                        |__anterior segment dysgenesis 1 1 rec.
                        |__anterior segment dysgenesis 2 3 rec.
                        |__anterior segment dysgenesis 3 1 rec.
                        |__anterior segment dysgenesis 4 1 rec.
                        |__anterior segment dysgenesis 5 2 rec.
                        |__anterior segment dysgenesis 6 2 rec.
                        |__anterior segment dysgenesis 7 7 rec.
                        |__anterior segment dysgenesis 8 3 rec.
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Is a monogenic disease
eye disease
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Synonyms
  • "anterior segment developmental anomaly" EXACT
    "corneal opacification and other ocular anomalies" EXACT
    "sclerocornea with other ocular anomalies" EXACT
Secondary IDs
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GARD:10025
ICD10CM:Q13.8
MIM:PS107250
ORDO:88632