Oklahoma Newborn Screening
Phone: 405-426-8220
Phone (alt.): 800-766-2223
FAX: 405-900-7556
Email: newbornscreen@health.ok.gov
Oklahoma Newborn Screening Website
Total number of conditions screened in this state: 56
2-methyl-3-hydroxybutyric aciduria2-methylbutyrylglycinuria
3-hydroxy-3-methylglutaric aciduria
3-methylcrotonyl-CoA carboxylase deficiency
3-methylglutaconic aciduria
Argininemia
Argininosuccinic aciduria
Benign hyperphenylalaninemia
Beta ketothiolase deficiency
Biopterin defect in cofactor biosynthesis
Biopterin defect in cofactor regeneration
Biotinidase deficiency
Carnitine acylcarnitine translocase deficiency
Carnitine palmitoyltransferase I deficiency
Carnitine palmitoyltransferase II deficiency
Carnitine uptake defect
Citrullinemia type I
Citrullinemia type II
Classic galactosemia
Congenital adrenal hyperplasia
Congenital hypothyroidism
Critical congenital heart disease
Cystic fibrosis
Glutaric acidemia type 1
Glutaric acidemia type II
Hearing
Hemoglobin SC disease
Holocarboxylase synthetase deficiency
Holocarboxylase synthetase deficiency (multiple carboxylase deficiency)
Homocystinuria
Hypermethioninemia
Isobutyrylglycinuria (Isobutyryl-CoA dehydrogenase deficiency)
Isovaleric acidemia
Long-chain L-3-hydroxyacyl- CoA dehydrogenase deficiency
Malonic acidemia
Malonic aciduria
Maple syrup urine disease
Medium-chain acyl-CoA dehydrogenase deficiency
Medium-chain ketoacyl-CoA thiolase deficiency
Methylmalonic acidemia
Mucopolysaccharidosis type 1
Phenylketonuria
Pompe
Propionic acidemia
Pyruvate carboxylase deficiency
Severe combined immunodeficiency
Short-chain acyl-CoA dehydrogenase deficiency
Sickle cell anemia (HbS/Beta zero thalassemia)
Sickle cell anemia (HbSS disease)
Spinal muscular atrophy
Trifunctional protein deficiency
Tyrosinemia type I
Tyrosinemia, type II
Tyrosinemia, type III
Very long-chain acyl-CoA dehydrogenase deficiency
X-linked adrenoleukodystrophy
Last Reviewed 03/01/2023
