An instance of retinal degeneration that is caused by an inherited modification of the individual's genome.
Comprehensive, easy-to-understand information about this condition
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apraxia
MONDO:0000665
peripheral retinal degeneration
MONDO:0001451
retinal dystrophies primarily involving Bruch's membrane
MONDO:0001666
vitreoretinal dystrophy
MONDO:0001923
dystrophies primarily involving the retinal pigment epithelium
MONDO:0001924
retinal dystrophy in systemic or cerebroretinal lipidoses
MONDO:0001925