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Retinitis pigmentosa 45

MONDO:0013413

Any retinitis pigmentosa in which the cause of the disease is a mutation in the CNGB1 gene.

Also known as: CNGB1 retinitis pigmentosa, RP45, retinitis pigmentosa 45, retinitis pigmentosa caused by mutation in CNGB1, retinitis pigmentosa type 45

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

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Broader categories

Disease (680) Nervous system disorder (231) Hereditary disease (176) Eye disorder (102) Retinal disorder (85) Retinitis pigmentosa (81) Inherited retinal dystrophy (40) Retinal degeneration (40) Perceptual disorders (22) Human disease (14)
Trials to join now! 12 Not yet recruiting 3 Not yet finished but already full! 1 Completed 8 Terminated 2
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  • Eye disease study lays groundwork for gene therapy breakthrough

    Knowledge-focused Terminated

    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

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