Diseases and Disorders > Pregnancy and Childbirth

Use these links to jump directly to your topic of interest in Pregnancy and Childbirth:

Pregnancy: Pregnancy (General) | Discomforts | Drugs | Exercise | Later-Age Pregnancy | Nutrition | Pregnancy Loss | Prenatal Tests | Risks to Pregnancy | Teenage Pregnancy

Childbirth: Birthing Options | Childbirth (Labor and Delivery) | Newborn Screening Tests | Multiple Births | Premature Birth | Postpartum Depression

Other Topics: General Pregnancy and Childbirth | Preparing for Pregnancy

Newborn Screening Tests

	General Information
	Newborn Screening Tests:Nemours Foundation
	Newborn Screening Tests:March of Dimes
	A Parent's Guide to Newborn Screening:Save Babies Through Screening [PDF]
	Newborn Screening Could Save Your Baby's Life:Oregon Dept of Human Services [PDF]
	About Expanded Newborn Screening:STAR-G Project
	See also Ears, Nose and Throat, Screening for Hearing Disorders
	Newborn Screening Fact Sheets:American Academy of Pediatrics [PDF]
	Newborn Screening:MedlinePlus
	National Newborn Screening Program
	National Newborn Screening and Genetics Resource Center (NNSGRC)
	National Newborn Screening Status Report [PDF]
	California Newborn Screening Program
	California Newborn Screening Program:California Department of Health Services

	Index to Disorders in National Newborn Screening Program
	Endocrine Disorders
	CAH:Congenital adrenal hyperplasia
	CH: Congenital hypothyroidism
	Hemoglobin Disorders
	Hb S/S: Sickle cell disease
	Hb S/A: Beta thalassemia
	Hb S/C: Hemoglobin C disease
	Other variant hemoglobinopathies (including Hb E)
	G6PD: Glucose 6 phosphate dehydrogenase
	Infectious Diseases
	HIV: Human immunodeficiency virus
	TOXO: Toxoplasmosis
	Metabolic, Amino Acid Disorders
	ARG: Arginemia (Arginase deficiency)
	ASA: Argininosuccinate acidemia
	BIOPT-BS: Defects of biopterin cofactor biosynthesis
	BIOPT-RG: Defects of biopterin cofactor regeneration
	CPS: Carbamoylphosphate synthetase
	CIT I: Citrullinemia type I (Argininosuccinate synthetase)
	CIT II: Citrullinemia type II
	HCY: Homocystinuria (cystathionine beta synthase)
	HHH: Ornithine translocase deficiency
	H-PHE: Benign hyperphenylalaninemia
	MET: Hypermethioninemia
	MSUD: Maple syrup urine disease (branched-chain ketoacid dehydrogenase )
	NKH: Nonketotic hyperglycinemia
	PKU: Phenylketonuria/ hyperphenylalaninemia
	PRO: Prolinemia
	TYR-I: Tyrosinemia Type I
	TYR-II: Tyrosinemia Type II
	TYR-III: Tyrosinemia Type III
	Metabolic, Carbohydrate Disorders
	GALT: Transferase deficient galactosemia (Classical)
	GALE: Galactose epimerase
	GALK: Galactokinase
	Metabolic, Fatty Acid Oxidation Disorders
	CACT: Carnitine acylcarnitine translocase
	CPT-Ia: Carnitine palmitoyltransferase Ia
	CPT-II: Carnitine palmitoyltransferase II
	CUD: Carnitine uptake defect (Carnitine transporter deficiency)
	De-Red: Dienoyl-CoA reductase
	EMA: Ethylmalonic encephalopathy
	GA-II: Glutaric acidemia type 2
	LCHAD: Long-chain hydroxyacyl-CoA dehydrogenase
	MAL: Malonic acidemia (Malonyl-CoA decarboxylase)
	MCAD: Medium-chain acyl-CoA dehydrogenase
	MCKAT: Medium-chain ketoacyl-CoA thiolase
	M/SCHAD: Medium/Short chain L-3-hydroxyacyl-CoA dehydrogenase
	SCAD: Short-chain acyl-CoA dehydrogenase
	TFP: Trifunctional protein
	VLCAD: Very long-chain acyl-CoA dehydrogenase
	Metabolic, Organic Acid Disorders
	2M3HBA: 2-Methyl-3-hydroxy butyric aciduria
	2MBCD: 2-Methylbutyryl-CoA dehydrogenase
	3MCC: 3-Methylcrotonyl-CoA carboxylase
	3MGA: 3-Methylglutaconic aciduria
	5-OXO: 5-oxoprolinuria (pyroglutamic aciduria)
	BKT: Beta ketothiolase
	GA-I: Glutaric acidemia type I
	HMG: 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency
	IBD: Isobutyryl-CoA dehydrogenase
	IVA: Isovaleric acidemia
	MCD: Multiple carboxylase (Holocarboxylase synthetase )
	MUT: Methylmalonic Acidemia (Methylmalonyl-CoA mutase Deficiency)
	CBL A,B: Methylmalonic acidemia (Cbl A, B)
	CBL C,D: Methylmalonic acidemia with Homocystinuria (Cbl C,D)
	PROP: Propionic acidemia (Propionyl-CoA carboxylase)
	Metabolic, Other
	BIO: Biotinidase
	Other Genetic Conditions
	CF: Cystic fibrosis
	Hearing loss

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