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Cone dystrophy

MONDO:0000455

An inherited ocular disorder characterized by the loss of cone cells, the photoreceptors responsible for both central and color vision.

Also known as: cone dystrophy, progressive cone dystrophy, stationary cone dystrophy, retinal cone dystrophy

28 clinical trials for this condition and its sub-types, 4 tagged with Cone dystrophy itself.

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Where it sits in the disease tree

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Part of

↑ Hereditary macular dystrophy (72)

Sub-types of Cone dystrophy

Cone dystrophy 3 0 trials
Cone dystrophy 4 0 trials
1 sub-type
- Achromatopsia 5 0 trials
Cone dystrophy with supernormal rod response 0 trials
Cone dystrophy, X-linked, with tapetal-like sheen 0 trials
Retinal cone dystrophy 4 0 trials
Retinal cone dystrophy type 1 0 trials

Including sub-types (28) Tagged with Cone dystrophy (4)

Trials to join now! 3 Terminated 1

Tiny genetic clues may unlock eye disease mysteries

Knowledge-focused Stopped early

This study looked at people with cone disorders, a type of inherited eye disease that affects color vision and sharp sight. Researchers analyzed genetic changes of unknown significance to see if they cause disease. The goal was to improve genetic diagnosis, not to test a treatmen…

Sponsor: University Hospital, Lille • Aim: Knowledge-focused

Last updated Jun 27, 2026 12:37 UTC