Michigan Newborn Screening Program
Phone: 866-673-9939
FAX: 517-335-9419
Email: newbornscreening@michigan.gov
Michigan Newborn Screening Program Website
Total number of conditions screened in this state: 59
2-methyl-3-hydroxy butyric aciduria2-methylbutyryl-CoA dehydrogenase deficiency
3-hydroxy 3-methylglutaric aciduria
3-methylcrotonyl-CoA carboxylase deficiency
3-methylglutaconic aciduria
Argininemia
Argininosuccinic acidemia
Benign hyperphenylalaninemia defect
Beta-ketothiolase deficiency
Biopterin cofactor biosynthesis defect
Biopterin cofactor regeneration defect
Biotinidase deficiency
Carnitine acylcarnitine translocase deficiency
Carnitine palmitoyltransferase I deficiency
Carnitine palmitoyltransferase II deficiency
Carnitine uptake deficiency
Citrullinemia type I
Citrullinemia type II
Congenital adrenal hyperplasia
Congenital hypothyroidism
Critical congenital heart disease
Cystic fibrosis
Dienoyl-CoA reductase deficiency
Galactosemia
Glutaric acidemia type I
Glutaric acidemia type II
Glycogen storage disease type II (Pompe)
Guanidinoacetate methyltransferase deficiency
Hearing loss
Hemoglobin H disease
Homocystinuria
Hypermethioninemia
Isovaleric acidemia
Long-chain L-3 hydroxy acyl-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-hydroxy acyl-CoA dehydrogenase deficiency
Methylmalonic acidemia cobalamin disorders
Methylmalonic acidemia methylmalonyl-CoA mutase
Methylmalonic acidemia with homocystinuria
Mucopolysaccharidosis type I
Multiple carboxylase deficiency
Phenylketonuria
Propionic acidemia
S/Beta thalassemia
S/C disease
Severe combined immunodeficiency
Sickle cell anemia
Spinal muscular atrophy
T-cell related lymphocyte deficiencies
Trifunctional protein deficiency
Tyrosinemia
Tyrosinemia type II
Tyrosinemia type III
Variant hemoglobinopathies
Very long-chain acyl-CoA dehydrogenase deficiency
X-linked adrenoleukodystrophy
Last Reviewed 03/01/2023
