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Wadsworth Center, Department of Health, New York StateD Wadsworth Center New York State Department of Health
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NYMAC
(New York-Mid-Atlantic Consortium for Genetics and Newborn Screening Services)

NYMAC Collaborative, New York-Mid-Atlantic Consortium for Genetic and Newborn Screening Services

NYMAC Region

NYMAC States

Map of the NYMAC States of NY, PA, NJ, DE, MD, WV, and VA

State Specific Resources for
People with Special Health
Care Needs

Emergency Cards

Amino Acidemias
ASA Argininosuccinic Aciduria
ADOHYC Adenosylhomocysteine Hydrolase Deficiency
ARG Argininemia or Arginase Deficiency
BH4 Tetrahydrobiopterin Deficiency
BKT Beta-Ketothiolase Deficiency
CIT-I Citrullinemia Type I
CIT-II Citrullinemia Type II
CBLAB Cobalamin A or B
CBLCDE Cobalamin C, D or E
GNMT Glycine N-Methyltransferase Deficiency
HMET Hypermethioninemia
HMG 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency
HCY Homocystinuria AKA Cystathionine B-Synthase Deficiency
MSUD Maple Syrup Urine Disease
PC Pyruvate Carboxylase Deficiency
PKU Phenylketonuria
TYR-I Tyrosinemia Type I (TYR-I) or Fumarylacetoacetate Hydrolase Deficiency (FAH)
TYR-II Tyrosinemia Type II
TYR-III Tyrosinemia Type III
Endocrine Disorders
CAH Congenital Adrenal Hyperplasia
CH Congenital Hypothyroidism
Fatty Acid Oxidation Disorders
CACT Carnitine/Acylcarnitine Translocase Deficiency
CPT1 Carnitine Palmitoyl Transferase Type 1 Deficiency
CPT2 Palmitoyl Transferase Type II Deficiency
CUD Carnitine Uptake Defect
EMA Ethylmalonic Encephalopathy
IBG Isobutyryl-CoA Dehydrogenase Deficiency
LCHAD Long-chain 3-Hydroxyacyl-CoA Dehydrogenase Deficiency
MCAD Medium-chain Acyl-CoA Dehydrogenase Deficiency
M-SCHAD Medium/Short-chain Hydroxyl-CoA Dehydrogenase Deficiency
SCAD Short-chain Acyl-CoA Dehydrogenase Deficiency
VLCAD Very Long-chain Acyl-CoA Dehydrogenase Deficiency
Hemoglobin Disorders
HBSB0 Sickle Beta-Zero Thalassemia
HBSB+ Sickle Beta-Plus Thalassemia
HBSC Sickle C Disease
HBSS Sickle Cell Disease
Organic Acidemias
2M3HBA 2-Methyl-3-Hydroxybutyric Acidemia
3MCC 3-Methylcrotonyl-CoA Carboxylase Deficiency
3MGA 3-Methylglutaconic Aciduria
GA-1 Glutaric Acidemia Type 1
IVA Isovaleric Acidemia
MA Malonic Acidemia (MA) or Malonyl-CoA Decarboxylase Deficiency
MADD Glutaric Aciduria Type 2 (GA2) or Multiple Acyl-CoA Dehydrogenase Deficiency (MADD)
MCD Holocarboxylase Deficiency (HCSD) or Multiple Carboxylase Deficiency (MCD)
MMA Methylmalonic Acidemia
PA Propionic Acidemia
TFP Trifunctional Protein Deficiency
Other
BIOT Biotinidase Deficiency
CF Cystic Fibrosis
GALT Galactosemia