Cure My Disease

Don't miss your cure!

Home News Browse Soon ready About
Log in / Sign up

CYP1B1-related glaucoma with or without anterior segment dysgenesis

MONDO:0800472

Any primary congenital glaucoma in which the cause of the disease is a mutation in the CYP1B1 gene.

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

Follow this condition — get notified about new trials

Sub-types

Anterior segment dysgenesis 6 (1) Glaucoma 3A (1)

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! 2 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