New Mexico Newborn Genetic Screening Program
Phone: 505-476-8858
Phone (alt.): 877-890-4692
Email: carlaa.ortiz@state.nm.us
New Mexico Newborn Genetic Screening Program Website
Total number of conditions screened in this state: 52
2-methyl-3-hydroxybutyryl CoA dehydrogenase deficiency2-methylbutyryl CoA dehydrogenase deficiency
3-hydroxy-3-methylglutaryl CoA lyase deficiency
3-methylcrotonyl CoA carboxylase deficiency
3-methylglutaconyl CoA hydratase deficiency
Arginase deficiency
Argininosuccinate lyase deficiency
Beta-ketothiolase deficiency
Biotinidase deficiency
Carnitine acylcarnitine translocase deficiency
Carnitine palmitoyl transferase deficiency, type I
Carnitine palmitoyl transferase deficiency, type II
Carnitine uptake defect
Citrullinemia, type I
Congenital adrenal hyperplasia
Critical congenital heart disease
Cystic fibrosis
Fabry
Galactosemia
Gaucher
Glutaric acidemia type II
Glutaric acidemia, type I
Hearing deficiency
Hemoglobinopathies
Homocystinuria
Hypermethioninemia
Isobutyryl-CoA dehydrogenase deficiency
Isovaleric acidemia
Long chain 3 hydroxyacyl-CoA dehydrogenase deficiency
Malonic acidemia
Maple syrup urine disease
Medium chain acyl-CoA dehydrogenase deficiency
Methylmalonic acidemia (cobalamin disorders)
Methylmalonic acidemia (methylmalonyl-CoA mutase deficiency)
Methylmalonic acidemia with homocystinuria
Mucopolysaccharidosis type I
Multiple carboxylase deficiency
Phenylketonuria
Pompe
Primary congenital hypothyroidism
Propionic acidemia
S, Beta-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
Last Reviewed 03/01/2023
