Cure My Disease

Don't miss your cure!

Home News Browse Soon ready About
Log in / Sign up

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

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

Follow this condition — get notified about new trials

Broader categories

Disease (680) Glaucoma (196) Hereditary disease (176) Eye disorder (102) Human disease (14) Congenital glaucoma (6) Disorder of orbital region (3) Disease of genetic or genomic mechanism (2) Primary congenital glaucoma (2) Disorder of visual system (1)
Trials to join now! 1 Not yet recruiting 1 Not yet finished but already full! 1 Completed 2 Terminated 1
Sort by
  • Can your phone spot eye cancer? app tested for retinoblastoma

    Diagnosis Terminated

    This study tested a smartphone app called CRADLE that uses a photo to detect leukocoria (a white glow in the pupil), which can be a sign of retinoblastoma, cataracts, or glaucoma. Researchers planned to compare the app's accuracy to a standard eye exam in children with these cond…

    Phase: NA • Sponsor: St. Jude Children's Research Hospital • Aim: Diagnosis

    Last updated Jun 27, 2026 12:07 UTC

Cure My Disease

Helping patients find clinical trials that match their disease.

Why was Cure my disease built?

Explore

Home News Browse About Terms of use Contact us

This is a site from Cyber and Space