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.
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retinal dystrophies primarily involving Bruch's membrane
MONDO:0001666
vitreoretinal dystrophy
MONDO:0001923
dystrophies primarily involving the retinal pigment epithelium
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retinal dystrophy in systemic or cerebroretinal lipidoses
MONDO:0001925
age-related macular degeneration
MONDO:0005150
helicoid peripapillary chorioretinal degeneration
MONDO:0007176