Cat-Map (https://cat-map.wustl.edu/home/cat-map-variant-file/-August (accessed on 1 August 2020)) reports 22 variants of EPHA2 associated with congenital cataracts (OMIM #116600) through autosomal dominant and recessive inheritance, in addition to sporadic mutations. Here, EPHA2 is linked to early-onset non-syndromic cataract.