New Hampshire Newborn Screening Program
Phone: 603-271-4225
FAX: 603-271-4519
Email: MCH@dhhs.nh.gov
New Hampshire Newborn Screening Program Website
Total number of conditions screened in this state: 40
3-hydroxy-3-methyl gluteric aciduria3-methylcrotonyl-CoA carboxylase deficiency
Argininemia
Argininosuccinic acidemia
Biotinidase deficiency
Carnitine palmitoyltransferase II deficiency
Carnitine uptake defect
Citrullinemia, type I
Cobalamin A, B
Congenital adrenal hyperplasia
Congenital hypothyroidism
Congenital toxoplasmosis
Critical congenital heart disorder
Cystic fibrosis
Galactosemia
Glutaric acidemia type I
Hearing loss
Hemoglobinopathies Hb S/BTh
Hemoglobinopathies Hb S/C
Hemoglobinopathies Hb SS
Homocystinuria
Hyperornithinemia-hyperammonemia-homocitrullinuria syndrome
Isovaleric acidemia
Long-chain L-3-OH acyl-CoA dehydrogenase deficiency
Maple syrup urine disease
Medium-chain acyl-CoA dehydrogenase deficiency
Methylmalonic acidemia: mutase deficiency
Mitochondrial acetoacetyl-CoA thiolase deficiency
Mucopolysaccharidosis type 1
Multiple acyl-CoA dehydrogenase deficiency
Multiple carboxylase deficiency
Phenylketonuria
Pompe disease
Propionic acidemia
Severe combined immunodeficiency
Spinal muscular atrophy
Trifunctional protein deficiency
Tyrosinemia type 1
Very long chain acyl-CoA dehydrogenase deficiency
X-linked adrenoleukodystrophy
Last Reviewed 03/01/2023
