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Maryland Department of Health
Genetics
Genetics
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Sickle Cell Disease
What is Sickle Cell Disease?
What is Sickle Cell Trait?
How can SCT impact a person’s health?
What do I need to know about SCT and sports?
How is Sickle Cell Trait (SCT) Inherited?
What does the Maryland Department of Health’s Sickle Cell Disease Follow-Up Program do?
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Office for Genetics and People with Special Health Care Needs
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Alphabetical List of Disorders on the Newborn Screen
Argininemia (Arginase deficiency)
Argininosuccinate aciduria
Beta Ketothiolase (Mitochondrial Acetyl-CoA Thiolase Deficiency
Biotinidase Deficiency
Carnitine Acyl-Carnitine Translocase Deficiency
Carnitine Palmitoyltransferase Deficiency Type 1 (CPT I)
Carnitine Palmitoyltransferase Deficiency Type 1 CPT II
Carnitine Uptake Deficiency
Citrullinemia
Cobalamin C deficiency
Congenital Adrenal Hyperplasia
Congenital Hypothyroidism
Cystic Fibrosis
2,4-dienoyl-CoA Reductase
Galactosemia
Glutaric Acidemia
Glutaric Acidemia Type II
Homocystinuria
3-Hydroxy-3Methylglutaric aciduria
Isobutyryl-CoA Dehydrogenase Deficiency
Isovaleric Acidemia
Long chain 3-hydroxyacyl-CoA dehydrogenase deficiency (LCHADD)
Malonic Acidemia
Maple syrup urine disease (Branched-chain ketoacid dehydrogenase deficiency)
Medium chain acyl-CoA dehydrogenase deficiency (MCADD)
2-Methyl-3Hydroxybutyryl-CoA Dehydrogenase Deficiency
2-Methylbutyryl-CoA Dehydrogenase Deficiency
3 Methylcrotonyl- CoA carboxylase deficiency (3-MCC)
Methylmalonic Acidemia
Multiple Carboxylase Deficiency
Phenylketonuria/ hyperphenylalaninemia
Propionic Acidemia
Short chain acyl-CoA dehydrogenase deficiency (SCADD)
Short chain 3-hydroxyacyl-CoA dehydrogenase deficiency (SCHADD)
Sickle Cell Anemia
Trifunctional Protein Deficiency
Tyrosinemia Type I
Tyrosinemia Type I/II/III
Very long chain acyl-CoA Dehydrogenase (VLCADD)
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