Oregon

Northwest Regional Newborn Screening Program
Phone: 503-693-4174
FAX: 503-693-5601
Email: NWRegional.NBS@state.or.us\

Northwest Regional Newborn Screening Program Website

 

Total number of conditions screened in this state: 62

2,4 Dienoyl-CoA reductase deficiency
2-methyl-3-hydroxybutyryl CoA dehydrogenase deficiency
2-methylbutyrylglycinuria
3-hydroxy-3-methylglutaryl CoA lyase deficiency
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 type II deficiency
Carnitine uptake defect
Citrullinemia, type I
Citrullinemia, type II
Congenital adrenal hyperplasia
Critical congenital heart disease
Cystic fibrosis
Fabry
Galactoepimerase deficiency
Galactokinase deficiency
Galactosemia
Gaucher
Glutaric acidemia type I
Glutaric acidemia, type II
Hearing loss
Hemoglobinopathies
Holocarboxylase synthetase deficiency
Homocystinuria
Hypermethioninemia
Isobutyrylglycinuria
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-hydroxyaxl-CoA dehydrogenase deficiency
Methylmalonic acidemia (cobalamin disorders)
Methylmalonic acidemia (methylmalonyl-CoA mutase deficiency)
Methylmalonic acidemia with homocystinuria
MPS-I
Phenylketonuria
Pompe
Primary congenital hypothyroidism
Propionic acidemia
S, Beta-thalassemia
S, C disease
Severe combined immunodeficiency
Short-chain acyl-CoA dehydrogenase deficiency
Sickle cell anemia
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