Figure 4 of Sun, Mol Vis 2020; 26:588-602.

Figure 4. Proportion of diseases associated with the six genes. A: ACHM is the most common disease in families carrying potential pathogenic variants (PPVs) in the six genes. B: Frequency of each gene in families with different diseases. PPVs in CNGB3 were the most common in families with ACHM. PPVs in CNGA3 were most common in families with CORD. ACHM, achromatopsia; CORD, cone-rod dystrophy; UN, unclassified retinopathy; LCA, Leber congenital amaurosis, OT, oligocone trichromacy; MD, macular degeneration; RP, retinitis pigmentosa; eoHM, early-onset high myopia; CSNB, congenital stationary night blindness.