Glucose‐6‐phosphate dehydrogenase (G6PD) deficiency is a genetic disorder that results in an inadequate amount of G6PD enzyme in red blood cells (RBC), a biological catalyst that is important to produce the reduced form of Nicotinamide Adenine Dinucleotide Phosphate (NADP) that protects red blood cells against oxidative stress [1]. Here, G6PD is linked to hereditary disease.