An inherited retinopathy caused by bi-allelic variants in the RP1 gene.
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autosomal dominant polycystic liver disease
MONDO:0000447
retinal dystrophies primarily involving Bruch's membrane
MONDO:0001666
tuberous sclerosis
MONDO:0001734
vitreoretinal dystrophy
MONDO:0001923
dystrophies primarily involving the retinal pigment epithelium
MONDO:0001924
retinal dystrophy in systemic or cerebroretinal lipidoses
MONDO:0001925