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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

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

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Sub-types

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

Broader categories

Disease (618) Nervous system disorder (217) Hereditary disease (172) Eye disorder (97) Retinal disorder (79) Inherited retinal dystrophy (40) Retinal degeneration (40) Perceptual disorders (21) Human disease (14) Hereditary neurological disease (5)
Trials to join now! 23 Not yet recruiting 3 Not yet finished but already full! 1 Completed 6 Terminated 3
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