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CNGB1-related retinopathy

MONDO:0800403

An inherited retinopathy caused by bi-allelic variants in the CNGB1 gene.

26 clinical trials for this condition and its sub-types, 0 tagged with CNGB1-related retinopathy itself.

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Where it sits in the disease tree

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Part of

↑ Inherited retinal dystrophy (513)

Sub-types of CNGB1-related retinopathy

Retinitis pigmentosa 45 1 trial

Including sub-types (26) Tagged with CNGB1-related retinopathy (0)

Trials to join now! 11 Not yet recruiting 3 Not yet finished but already full! 1 Completed 9 Terminated 2

Eye disease study lays groundwork for gene therapy breakthrough

Knowledge-focused Paused

This study looks at a rare, inherited eye disease called CNGB1 retinitis pigmentosa that causes gradual vision loss and blindness. Researchers want to learn how the disease progresses by using eye exams and imaging tests over three years. The goal is to find the best ways to meas…

Sponsor: Columbia University • Aim: Knowledge-focused

Last updated Jun 27, 2026 12:06 UTC