Section 181-2-003 - SPECIFICATION OF DISEASESAll infants born in the state of Nebraska must be tested for the diseases identified in Neb.Rev.Stat. § 71-519 and the following diseases:
(1) Argininosuccinic Acidemia (beginning July 1, 2008);(2) Beta-ketothiolase Deficiency (beginning July 1, 2008);(3) Carnitine Uptake Defect (beginning July 1, 2008);(4) Citrullinemia (beginning July 1, 2008);(5) Congenital Adrenal Hyperplasia;(7) Glutaric Acidemia type 1 (beginning July 1, 2008);(8) Homocystinuria (beginning July 1, 2008);(9) Isovaleric Acidemia (beginning July 1, 2008);(10) Long-chain Hydroxyacyl-CoA Dehydrogenase Deficiency (beginning July 1, 2008);(11) Maple Syrup Urine Disease (beginning July 1, 2008);(12) Methylmalonic Acidemia (Mutase Deficiency) (beginning July 1, 2008);(13) Methylmalonic Acidemia (Cbl A and B) (beginning July 1, 2008);(14) Multiple Carboxylase Deficiency (beginning July 1, 2008);(15) Propionic Acidemia (beginning July 1, 2008);(16) Severe Combined Immune Deficiencies (beginning 45 days after the effective date of this regulation) (17) Tyrosinemia (beginning July 1, 2008);(18) Trifunctional Protein Deficiency (beginning July 1, 2008);(19) Very Lng-chain Acyl-CoA Dehydrogenase Deficiency (beginning July 1, 2008);(20) 3-Hydroxy 3-Methyl Glutaric Aciduria (beginning July 1, 2008); and(21) 3-Methylcrotonyl-CoA Carboxylase Deficiency (beginning July 1, 2008).181 Neb. Admin. Code, ch. 2, § 003
Adopted effective 6/5/2018Amended effective 9/21/2020