Nebraska Newborn Screening
Phone: 402-471-6733
Phone (alt.): 800-664-7772
FAX: 402-742-2332
Email: DHHS.newbornscreening@nebraska.gov
Nebraska Newborn Screening Website
Total number of conditions screened in this state: 38
3-hydroxy 3-methyl glutaric aciduria3-methylcrotonyl-CoA carboxylase deficiency
Argininosuccinic acidemia
Beta ketothiolase deficiency
Biotinidase deficiency
Carnitine update defect
Citrullinemia
Congenital adrenal hyperplasia
Congenital primary hypothyroidism
Critical congenital heart disease
Cystic fibrosis
Galactosemia
Glutaric acidemia type 1
Hearing loss
Hemoglobinopathies
Homocystinuria
Isovaleric acidemia
Long-chain hydroxyacyl-CoA dehydrogenase deficiency
Maple syrup urine disease
Medium chain acyl CoA dehydrogenase deficiency
Methylmalonic acidemia (cobalamin disorders)
Methylmalonic acidemia (methylmalonyl-CoA mutase)
Mucopolysaccharidosis type 1
Multiple carboxylase deficiency
Phenylketonuria
Pompe diseases
Propionic acidemia
Severe combined immune deficiency
Sickle beta thalassemia
Sickle cell disease
Sickle hemoglobin C disease
Spinal muscular atrophy
Trifunctional protein deficiency
Tyrosinemia type I
Tyrosinemia, type II
Tyrosinemia, type III
Very long-chain acycl-CoA dehydrogenase deficiency
X-linked adrenoleukodystrophy
Last Reviewed 03/01/2023