Anterior Segment Dysgenesis

Alias:

Anterior Segment Developmental Anomaly

Corneal Opacification and Other Ocular Anomalies

Sclerocornea with Other Ocular Anomalies

Anterior Segment Mesenchymal Dysgenesis

Axenfeld-Rieger Syndrome, Type 3

Dysgenesis, Anterior Segment

Irido-Corneal Dysgenesis

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Basic Information

Medical Symptom

Gene & Mutation

Related Drugs

Disease Model

References Literature

Anterior Segment Dysgenesis, also known as anterior segment developmental anomaly, is related to anterior segment dysgenesis 5 and anterior segment dysgenesis 2. An important gene associated with Anterior Segment Dysgenesis is FOXE3 (Forkhead Box E3), and among its related pathways/superpathways are Mesodermal commitment pathway and Transcriptional Regulatory Network in Embryonic Stem Cell. Affiliated tissues include eye and retina, and related phenotypes are nervous system and pigmentation

Related ID：

MALACARDS：ANT088

ICD11：1182282997