Alphabetic list of conditions included in the Ohio Newborn Screening Panel

Argininemia (ARG)
Argininosuccinic Acidemia (ASA)
Biotinidase Deficiency (BIOT)
Carnitine Acylcarnitine Translocase Deficiency (CACT)
Carnitine Palmitoyl Transferase Deficiency Type II (CPT-II)
Carnitine Uptake Defect (CUD)
Citrullinemia Type I (CIT) and Citrullinemia Type II (CIT II)
Congenital Adrenal Hyperplasia (CAH)
Congenital Hearing Loss
Primary Congenital Hypothyroidism
Critical Congenital Heart Defects (CCHD)
Cystic Fibrosis (CF)
Duchenne Muscular Dystrophy
Galactosemia (GALT)
Glutaric Acidemia Type I (GA-1)
Glutaric Acidemia Type II (GA-2)
Glycogen Storage Disease Type II (Pompe Disease)
Homocystinuria (HCY)
3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency (HMG)
Hypermethioninemia (MET)
Isovaleric Acidemia (IVA)
Krabbe Leukodystrophy
3-Ketothiolase Deficiency (BKT)
Long-Chain Hydroxyacyl-CoA Dehydrogenase Deficiency (LCHAD)
Maple Syrup Urine Disease (MSUD)
Medium-Chain Acyl-CoA Dehydrogenase Deficiency (MCAD)
2-Methylbutyryl-CoA Dehydrogenase Deficiency (2MBG)
3-Methylcrotonyl-CoA Carboxylase Deficiency (3-MCC)
Methylmalonic Acidemia
- Cobalamin Disorders A and B (Cbl A,B)
- Methylmalonyl-CoA Mutase Deficiency (MUT)
- Methylmalonic Acidemia with Homocystinuria (Cbl C, D, F)
Mucopolysaccharidosis type I (MPS I)
Multiple CoA Carboxylase Deficiency (MCD)
Phenylketonuria (PKU)
Propionic Acidemia (PROP)
Severe Combined Immunodeficiency (SCID)
Sickle Cell Disease (Hb SS) and other Hemoglobinopathies (e.g. SC Disease, Sickle Beta-Thalassemia)
Spinal muscular atrophy (SMA)
Trifunctional Protein Deficiency (TFP)
Tyrosinemia Type I (TYR I), Type II (TYR II) and Type III (TYR III)
Very Long-Chain Acyl-CoA Dehydrogenase Deficiency (VLCAD)
X-Linked Adrenoleukodystrophy (X-ALD)