1.6	List of Conditions for Newborn Screening
1.6.1	The Laboratory shall conduct screening tests for the following conditions:
1.6.1.1		Phenylketonuria
1.6.1.2		Congenital Hypothyroidism
1.6.1.3		Hemoglobinopathies
1.6.1.4		Galactosemia
1.6.1.5		Cystic Fibrosis
1.6.1.6		Biotinidase Deficiency
1.6.1.7		Congenital Adrenal Hyperplasia
1.6.1.8		Medium Chain Acyl-CoA dehydrogenase deficiency
1.6.1.9		Very Long Chain Acyl-CoA dehydrogenase deficiency
1.6.1.10	Long-Chain L-3-Hydroxy Acyl-CoA dehydrogenase deficiency
1.6.1.11	Trifunctional protein deficiency
1.6.1.12	Carnitine Acyl-carnitine translocase deficiency
1.6.1.13	Short Chain Acyl-CoA dehydrogenase deficiency
1.6.1.14	Carnitine palmitoyltransferase II deficiency
1.6.1.15	Glutaric acidemia Type 2
1.6.1.16	Arginosuccinic acidemia
1.6.1.17	Citrullinemia
1.6.1.18	Tyrosinemia
1.6.1.19	Hypermethionemia
1.6.1.20	Maple Syrup urine disease
1.6.1.21	Homocystinuria
1.6.1.22	Isovaleric acidemia
1.6.1.23	Glutaric acidemia Type 1
1.6.1.24	3-hydroxy-3-methylglutaryl-CoA Lyase deficiency
1.6.1.25	Multiple Carboxylase deficiency
1.6.1.26	3-methylcrotonyl-CoA carboxylase deficiency
1.6.1.27	3-methylglutaconic aciduria
1.6.1.28	Methylmalonic acidemias
1.6.1.29	Propionic acidemia
1.6.1.30	beta-Ketothiolase deficiency
1.6.1.31	Carnitine uptake defect 
1.6.1.32	Arginase deficiency 
1.6.1.33	Malonic acidemia 
1.6.1.34	Carnitine palmitoyltransferase deficiency 1A