Rare biallelic DRAM2 variants causing putative loss of DRAM2 function have been associated with retinal dystrophy (El-Asrag et al., 2015; Sergouniotis et al., 2015; Birtel et al., 2018; Kuniyoshi et al., 2020; Krašovec et al., 2022). The gene discussed is DRAM2; the disease is inherited retinal dystrophy.