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Anterior segment dysgenesis 3

MONDO:0024456

An iridogoniodysgenesis that results from alterations in the forkhead transcription factor gene (FOXC1)

Also known as: ASGD3, FOXC1 iridogoniodysgenesis, IGDA, IGDA syndrome, IRID1, anterior segment dysgenesis 3, anterior segment dysgenesis 3, multiple subtypes, iridogoniodysgenesis anomaly, autosomal dominant

13 clinical trials for this condition and its sub-types.

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Broader categories

Disease (618) Glaucoma (177) Hereditary disease (172) Eye disorder (97) Human disease (14) Disorder of orbital region (3) Anterior segment dysgenesis (2) Disease of genetic or genomic mechanism (2) Disorder of visual system (1) Uveal disorder (1)
Trials to join now! 8 Not yet finished but already full! 3 Completed 1 Terminated 1
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  • App aims to clear up glaucoma drop confusion

    Knowledge-focused Completed

    This study tested whether a simple app, available in English, Spanish, and Cantonese, could help glaucoma patients better remember their multiple eye drop schedules. Twenty participants either used the app or received standard instructions. After one month, researchers compared h…

    Phase: NA • Sponsor: University of California, San Francisco • Aim: Knowledge-focused

    Last updated Jun 27, 2026 08:07 UTC

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