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Cone-rod dystrophy 18

MONDO:0014153

Any cone-rod dystrophy in which the cause of the disease is a mutation in the RAB28 gene.

Also known as: CORD18, RAB28 cone-rod dystrophy, cone-rod dystrophy 18, cone-rod dystrophy caused by mutation in RAB28, cone-rod dystrophy type 18

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

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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) Cone-rod dystrophy (16) Human disease (14)
Trials to join now! 21 Not yet recruiting 3 Not yet finished but already full! 1 Completed 6 Terminated 2
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