Any Leber congenital amaurosis in which the cause of the disease is a mutation in the CRX gene.
Comprehensive, easy-to-understand information about this condition
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Gene data from MyGene.info • Click to view on NCBI Gene
cone-rod dystrophy 2
MONDO:0007362
retinal aplasia
MONDO:0008372
Leber congenital amaurosis 1
MONDO:0008764
Leber congenital amaurosis 2
MONDO:0008765
Leber congenital amaurosis 3
MONDO:0011415
Leber congenital amaurosis 4
MONDO:0011458