Utah Newborn Screening
Phone: 801-584-8256
FAX: 801-536-0966
Utah Newborn Screening Website
Total number of conditions screened in this state: 61
2-methylbutyryl CoA dehydrogenase deficiency2M3HBA Deficiency
3-hydroxy-3-methylglutaryl-CoA lyase deficiency
3-methylglutaconic aciduria
3MCC deficiency
Arginase deficiency
Argininosuccinate lyase deficiency
Argininosuccinic acidemia
Beta-ketothiolase deficiency
Biopterin defect in cofactor biosynthesis
Biopterin defect in cofactor regeneration
Biotinidase deficiency
CACT Deficiency
Carnitine uptake defect/transport defect
Carnitine-acylcarnitine translocase deficiency
Citrullinemia, type I
Citrullinemia, type II
Congenital adrenal hyperplasia
Congenital hypothyroidism
CPT1 Deficiency
CPT2 Deficiency
Critical congenital heart disease
Cystic fibrosis
Galactosemia
GAMT Deficiency
Glutaric acidemia type 2
Glutaric Acidemia, Type 2
Glutaric acidemia, type I
Hearing loss
Hemoglobin C, D, and E disorders
Hemoglobin trait (C, D, E, or Unidentified)
Homocystinuria
Hyperprolinemia type I
Hyperprolinemia type II
Isobutyrylglycinuria
Isovaleric acidemia
LCHAD Deficiency
Malonic acidemia
Maple syrup urine disease
MCAD Deficiency
Methylmalonic acidemia (cobalamin disorders)
Methylmalonic acidemia (mutase deficiency)
Methylmalonic acidemia with homocystinuria
Multiple carboxylase deficiency
PKU
Propionic acidemia
Pyruvate carboxylase deficiency
S,C disease
S,S disease (sickle cell anemia)
SCAD Deficiency
SCHAD deficiency
Severe combined immune deficiency
Sickle cell disease
Sickle cell trait
Spinal muscular atrophy
TFP deficiency
Tyrosinemia, type I
Tyrosinemia, type II
Tyrosinemia, type III
VLCAD Deficiency
X-linked adrenoleukodystrophy
Last Reviewed 03/01/2023
