North Dakota Newborn Screening Program
Phone: 701-328-4534
Email: jbmeyer@nd.gov
North Dakota Newborn Screening Program Website
Total number of conditions screened in this state: 52
2-methyl-3-hydroxybutyric acidemia2-methylbutyrylglycinuria
3-hydroxy 3-methylglutaric aciduria
3-methylcrotonyl-CoA carboxylase deficiency
3-methylglutaconic aciduria
Argininemia
Argininosuccinic aciduria
Benign hyperphenylalaninemia
Biopterin defect in cofactor biosynthesis
Biopterin defect in cofactor regeneration
Biotinidase deficiency
Carnitine acylcarnitine translocase deficiency
Carnitine palmitoyltransferase type I deficiency
Carnitine palmitoyltransferase type II deficiency
Carnitine uptake defect
Citrullinemia, type I
Citrullinemia, type II
Classic galactosemia
Classic phenylketonuria
Congenital adrenal hyperplasia
Critical congenital heart disease
Cystic fibrosis
Glutaric acidemia, type I
Glutaric acidemia, type II
Hearing loss
Holocarboxylase synthase deficiency
Homocystinuria
Hypermethioninemia
Isovaleric acidemia
Long-chain L-3 hydroxyacyl-CoA dehydrogenase deficiency
Malonic acidemia
Maple syrup urine disease
Medium-chain acyl-CoA dehydrogenase deficiency
Medium-chain ketoacyl-CoA thiolase deficiency
Medium/short-chain L-3-hydroxyacyl-CoA dehydrogenase deficiency
Methylmalonic acidemia (cobalamin disorders)
Methylmalonic acidemia (methylmalonyl-CoA mutase)
Methylmalonic acidemia with homocystinuria
Primary congenital hypothyroidism
Propionic acidemia
S, βeta-thalassemia
S,C disease
S,S disease (sickle cell anemia)
Severe combined immunodeficiency
Spinal muscular atrophy
Trifunctional protein deficiency
Tyrosinemia, type I
Tyrosinemia, type II
Tyrosinemia, type III
Variant hemoglobinopathies
Very long-chain acyl-CoA dehydrogenase deficiency
βeta-ketothiolase deficiency
Last Reviewed 03/01/2023
