RDH12-related dominant retinopathy

MONDO:0800100

A retinopathy caused by gain of function, heterozygous variants in the RDH12 gene, and associated with late onset retinopathy with a mild phenotype, characterized by nyctalopia and visual field loss, but relatively preserved central vision.

Also known as: RDH12-related dominant retinopathy

25 clinical trials for this condition and its sub-types, 0 tagged with RDH12-related dominant retinopathy itself.

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↑ Inherited retinal dystrophy (513)

Including sub-types (25) Tagged with RDH12-related dominant retinopathy (0)

We haven't found any trials for this condition yet. Follow it to get notified when new trials appear.