Minnesota Newborn Screening Program
Phone: 651-201-5466
Phone (alt.): 800-664-7772
FAX: 651-215-6285
Email: health.newbornscreening@state.mn.us
Minnesota Newborn Screening Program Website
Total number of conditions screened in this state: 63
2-methyl-3-hydroxybutyric acidemia2-methylbutyryl-CoA dehydrogenase deficiency
3-hydroxy-3-methylglutaryl-CoA lyase deficiency
3-methylcrotonyl-CoA carboxylase deficiency
3-methylglutaconyl-CoA hydratase deficiency
Alpha thalassemia major
Arginemia
Argininosuccinate acidemia
Beta ketothiolase deficiency
Biopterin defect in cofactor biosynthesis
Biopterin defect in cofactor regeneration
Biotinidase deficiency
Carnitine acylcarnitine translocase deficiency
Carnitine palmitoyltransferase deficiency I
Carnitine palmitoyltransferase deficiency II
Carnitine uptake defect
Citrullinemia type I
Citrullinemia type II
Congenital adrenal hyperplasia
Congenital hypothyroidism
Critical congenital heart disease
Cystic fibrosis
Dienoyl-CoA reductase deficiency
Galactoepimerase deficiency
Galactokinase deficiency
Galactosemia
Glutaric acidemia type I
Glutaric acidemia type II
Hearing loss
Hemoglobin H disease
Homocystinuria
Hypermethioninemia
Hyperphenylalaninemia
Isobutyryl-CoA dehydrogenase deficiency
Isovaleric acidemia
Long-chain hydroxyacyl-CoA dehydrogenase deficiency
Malonic acidemia
Maple syrup urine disease
Medium-chain acyl-CoA dehydrogenase deficiency
Medium-chain keto acyl-CoA thiolase deficiency
Medium/short-chain hydroxy acyl-CoA dehydrogenase deficiency
Methylmalonic acidemia (cobalamin disorders A and B)
Methylmalonic acidemia (mutase deficiency)
Methylmalonic acidemia with homocystinuria
Mucopolysaccharidosis type I
Multiple CoA carboxylase deficiency
Phenylketonuria
Pompe disease
Propionic acidemia
Severe combined immunodeficiency
Short-chain acyl-CoA dehydrogenase deficiency
Sickle cell disease
Sickle βeta-plus thalassemia
Sickle-C disease
Spinal muscular atrophy
T-cell lymphopenia
Trifunctional protein deficiency
Tyrosinemia type I
Tyrosinemia type II
Tyrosinemia type III
Variant hemoglobinopathies
Very long-chain acyl-CoA dehydrogenase deficiency
X-linked adrenoleukodystrophy
Last Reviewed 03/01/2023
