Sly Syndrome, Sucrase-Isomaltase Deficiency, Valproic Acid Metabolism Pathway, Tay-Sachs Disease, Sialuria or French Type Sialuria, Amino Sugar Metabolism, Salla Disease/Infantile Sialic Acid Storage Disease, G(M2)-Gangliosidosis: Variant B, Tay-Sachs Disease, Porphyria Variegata (PV), Congenital Erythropoietic Porphyria (CEP) or Gunther Disease, Acute Intermittent Porphyria, Hereditary Coproporphyria (HCP), and Porphyrin Metabolism (Figure 5C). This evidence concerns the gene SI and mucopolysaccharidosis type 7.