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Acylcarnitine Abnormalities - (Organic Acidemias and Fatty Acid Oxidation Disorders)
Amino Acid Abnormalities
Biotinidase Deficiency
Congenital Adrenal Hyperplasia (CAH)
Congenital Hypothyroidism
Cystic Fibrosis
Fabry Disease
Galactosemia
Mucopolysaccharidoses Type I - (MPS-I)
Pompe Disease - (Glycogen Storage Disease Type II)
Severe Combined Immunodeficiency Disorder
Spinal Muscular Atrophy