FH occurs widely because of mutation in the following genes: LDLR gene, apolipoprotein B (Apo B), proprotein convertase subtilisin/kexin type 9 (PCSK 9), LDLR adaptor protein 1 (LDLRAP1), and other unidentified genes [6]. The gene discussed is LDLRAP1; the disease is familial hyperaldosteronism.