Glycine N-methyltransferase Deficiency<\/td> | <\/a><\/a><\/a><\/td> | Not Available<\/span><\/td><\/tr>Homocystinuria-megaloblastic anemia due to defect in cobalamin metabolism, cblG complementation type<\/td> | <\/a><\/a><\/a><\/td> | Not Available<\/span><\/td><\/tr>Hyperglycinemia, non-ketotic<\/td> | <\/a><\/a><\/a><\/td> | Not Available<\/span><\/td><\/tr><\/tbody><\/table> | | |