Any cone dystrophy in which the cause of the disease is a mutation in the PDE6C gene.
Comprehensive, easy-to-understand information about this condition
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Gene data from MyGene.info • Click to view on NCBI Gene
retinal cone dystrophy type 1
MONDO:0008374
cone dystrophy, X-linked, with tapetal-like sheen
MONDO:0010567
cone dystrophy 3
MONDO:0011193
cone dystrophy with supernormal rod response
MONDO:0012475
retinal cone dystrophy 4
MONDO:0012507
achromatopsia 5
MONDO:0800196