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Leber congenital amaurosis 18

MONDO:1060145

A Leber congenital amaurosis that is caused by a variation in the PRPH2 gene.

Also known as: LCA18

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) Human disease (14) Hereditary neurological disease (5)
Trials to join now! 21 Not yet recruiting 3 Not yet finished but already full! 1 Completed 6 Terminated 2
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