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Cone-rod dystrophy 6

MONDO:0011143

Any cone-rod dystrophy in which the cause of the disease is a mutation in the GUCY2D gene.

Also known as: CORD6, GUCY2D cone-rod dystrophy, RCD2, cone-rod dystrophy 6, cone-rod dystrophy caused by mutation in GUCY2D, cone-rod dystrophy type 6, retinal cone dystrophy 2

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

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Broader categories

Disease (679) Nervous system disorder (231) Hereditary disease (176) Eye disorder (102) Retinal disorder (85) Inherited retinal dystrophy (40) Retinal degeneration (40) Perceptual disorders (22) Cone-rod dystrophy (16) 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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