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Glaucoma 3A

MONDO:0009277

An autosomal recessive form of congenital glaucoma caused by mutation(s) in the CYP1B1 gene, encoding cytochrome P450 1B1.

Also known as: buphthalmos, Primary Congenital glaucoma 3A, glaucoma 3, primary congenital, type a, glaucoma 3A, primary open angle, congenital, juvenile, or adult onset, GLC3A, glaucoma 3, primary congenital, A, glaucoma, congenital, glaucoma, primary open angle, adult-onset

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) Congenital glaucoma (5) Disorder of orbital region (3) Disease of genetic or genomic mechanism (2) Disorder of visual system (1) Primary congenital glaucoma (1)
Trials to join now! 8 Not yet finished but already full! 2 Completed 1 Terminated 2
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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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