ICD H35.5ORPHA:1872CRD

Cone-Rod Dystrophy

Cone-rod dystrophy is a group of inherited eye conditions that damage the light-sensing cells of the retina. The cones, which give sharp central and colour vision, are affected first, and the rods, which give night and side vision, later. Many different genes can cause it. Care focuses on low vision support, and gene-based therapies are being studied.

289
Articles
9
Trials (1 AU)
Updated
11 September 2026
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Common Questions

What is Cone-Rod Dystrophy?

Cone-rod dystrophy is a group of inherited eye conditions that damage the light-sensing cells of the retina. The cones, which give sharp central and colour vision, are affected first, and the rods, which give night and side vision, later. Many different genes can cause it. Care focuses on low vision support, and gene-based therapies are being studied.

How many clinical trials are available for Cone-Rod Dystrophy?

RareWays currently indexes 9 clinical trials for Cone-Rod Dystrophy, of which 7 are actively recruiting. Trial availability changes as new studies are registered — check the trials tab for current status.

Where does the research data for Cone-Rod Dystrophy come from?

RareWays aggregates research from PubMed, Europe PMC, OpenAlex, and ClinicalTrials.gov. Data is updated regularly by Rocky, RareWays' automated research engine. All articles and trials link directly to their original sources.

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This information is for general awareness only.

For guidance specific to your situation, please speak with your healthcare team.