A Leber congenital amaurosis that is caused by a variation in the PRPH2 gene.
Comprehensive, easy-to-understand information about this condition
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fundus albipunctatus
MONDO:0007639
patterned macular dystrophy 1
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retinal aplasia
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Leber congenital amaurosis 1
MONDO:0008764
Leber congenital amaurosis 2
MONDO:0008765
Leber congenital amaurosis 3
MONDO:0011415