Ohio

Ohio Newborn Screening
Phone: 888-634-5227
Phone (alt.): 614-466-4684
FAX: 614-644-4648
Email: ODHLabs@odh.ohio.gov

Ohio Newborn Screening Website

 

Total number of conditions screened in this state: 47

2-methylbutyryl-CoA dehydrogenase deficiency
3-hydroxy-3-methylglutaryl-CoA lyase deficiency
3-ketothiolase deficiency
3-methylcrotonyl-CoA carboxylase deficiency
Argininemia
Argininosuccinic acidemia
Biotinidase deficiency
Carnitine acylcarnitine translocase deficiency
Carnitine palmitoyl transferase deficiency type II
Carnitine uptake defect
Citrullinemia type I
Citrullinemia type II
Congenital adrenal hyperplasia
Congenital hearing loss
Critical congenital heart disease
Cystic fibrosis
Galactosemia
Glutaric acidemia type I
Glutaric acidemia type II
Glycogen storage disease type II (Pompe disease)
Hemoglobinopathies
Homocystinuria
Hypermethioninemia
Isovaleric acidemia
Krabbe leukodystrophy
Long-chain hydroxyacyl-CoA dehydrogenase deficiency
Maple syrup urine disease
Medium-chain acyl-CoA dehydrogenase deficiency
Methylmalonic acidemia with homocystinuria
Methylmalonic acidemia: Cobalamin disorders A and B
Methylmalonic acidemia: Methylmalonyl-CoA mutase deficiency
Mucopolysaccharidosis type I
Multiple CoA carboxylase deficiency
Phenylketonuria
Primary congenital hypothyroidism
Propionic acidemia
SC disease
Severe combined immunodeficiency
Sickle beta-thalassemia
Sickle cell disease
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