District of Columbia | Newborn Screening

State Newborn Screening Panel

2,4 Dienoyl-CoA reductase deficiency
2-methyl-3-hydroxybutyric aciduria
2-methylbutyrylglycinuria
3-hydroxy-3-methyglutaric aciduria
3-methylcrotonyl-CoA carboxylase deficiency
3-methylglutaconic aciduria
Adrenoleukodystrophy
Argininemia
Argininosuccinic aciduria
Benign hyperphenylalaninemia
Beta-ketothiolase deficiency
Biotinidase deficiency
Carbamoyl phosphate synthetase I 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
Galactoepimerase deficiency
Galactokinase deficiency
Glucose-6-phosphate dehydrogenase deficiency
Glutaric acidemia type I
Glutaric acidemia type II
Hearing loss
Hemoglobinopathies
Holocarboxylase synthase deficiency
Homocystinuria
Hypermethioninemia
Hyperornithine with gyrate deficiency
Hyperornithinemia-hyperammonemia-homocitrullinuria syndrome
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-hydroxyacyl-CoA dehydrogenase deficiency
Methylmalonic acidemia (cobalamin disorders)
Methylmalonic acidemia (methylmalonyl-CoA mutase)
Methylmalonic acidemia with homocystinuria (Cbl C,D)
Mucopolysaccharidosis type I
Pompe
Primary congenital hypothyroidism
Propionic acidemia
Pyroglutamic acidemia
S, βeta-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

Contacts and Support

State Newborn Screening Program

DC Newborn Screening Program

DC Newborn Screening Program Website

State Newborn Screening Program

DC Newborn Metabolic Screening Program (DC NMS Program)

Phone: 202-510-5335

FAX: 202-478-5813

Email: Danielle.Chapman2@dc.gov

DC Newborn Metabolic Screening Program Website

Critical Congenital Heart Disease Screening

DC Newborn Critical Congenital Heart Disease Screening Program (DC CCHD Program)

Phone: 202-510-5335

Email: Danielle.Chapman2@dc.gov

Early Hearing Detection and Intervention

DC Early Hearing Detection and Intervention Program (DC EHDI)

Phone: 202-934-3757

Email: emily.small@dc.gov

Additional Resources

For a listing of general support, advocacy, and informational resources for Newborn Screening, visit the Resources page.

Date Last Reviewed:

June 2025