Washington | Newborn Screening

State Newborn Screening Panel

3-hydroxy-3-methylglutaric aciduria
Alpha thalassemia (Barts)
Argininosuccinic acidemia
Beta thalassemia
Beta-ketothiolase deficiency
Biotinidase deficiency
Carnitine uptake deficiency
Citrullinemia
Congenital adrenal hyperplasia
Congenital hypothyroidism
Critical congenital heart disease
Cystic fibrosis
Galactosemia
Glutaric acidemia type I
Glygogen storage disorder type II
Hearing loss
Hemoglobin C trait
Hemoglobin D trait
Hemoglobin E trait
Hemoglobin S trait
Hemoglobin sickle C disease
Hemoglobinopathies
Homocystinuria
Isovaleric acidemia
Long-chain L-3-hydroxyacyl-CoA dehydrogenase deficiency
Maple syrup urine disease
Medium-chain acyl-CoA dehydrogenase deficiency
Methylmalonic acidemia (CblA, B)
Methylmalonic acidemia (mutase deficiency)
Mucopolysaccharidosis type I
Multiple carboxylase deficiency
Phenylketonuria
Propionic acidemia
Severe combined immunodeficiency
Sickle cell disease
Spinal muscular atrophy
Trifunctional protein deficiency
Tyrosinemia type 1
Very-long chain acyl-CoA dehydrogenase deficiency
X-linked adrenoleukodystrophy

In this state, babies undergo a second screening step when they are around two weeks old. This second screening usually happens in a health care provider’s office. It can help find babies who have conditions that are hard to detect in the first days of life but that still benefit from early treatment or intervention.

Contacts and Support

State Newborn Screening Program

Washington State Newborn Screening Program

Phone: 206-418-5410

Phone (alt.): 866-660-9050

FAX: 206-363-1610

Email: nbs.prog@doh.wa.gov

Washington State Newborn Screening Program Website

Early Hearing Detection and Intervention

Early Hearing Detection Intervention (EHDI)

Phone: 1-888-923-4334

Email: ehddi2@doh.wa.gov

Washington EHDI Program Website

Additional Resources

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

Date Last Reviewed:

September 2024