LOINC Chemistry codes
Chemistry (CHEM): one class of the LOINC code system.
10,855 codes · page 123 of 218 · every class · by category · by group · panels · answer lists · parts
Fibroblast growth factor 23 46699-5 7-Dehydrocholesterol (Amniotic Fluid) 46700-1 Adenosine triphosphate (Red Blood Cells) 46701-9 Ceruloplasmin (Dbs) 46716-7 Alpha-1-Microglobulin (Urine) 46723-3 Prolactin monomeric 46727-4 Amino acidemias newborn screen interpretation 46733-2 Citrullinemias/Arginosuccinic aciduria newborn screen interpretation 46734-0 Endocrine disorders newborn screen interpretation (qualitative) 46735-7 Fatty acid oxidation defects newborn screen interpretation 46736-5 Galactosemias newborn screen interpretation 46737-3 Genetic.Disorders newborn screen interpretation (qualitative) 46738-1 Glutaric acidemia type 1 newborn screen interpretation 46739-9 Hemoglobin disorders newborn screen interpretation 46740-7 Homocystinuria and/or other hypermethioninemias newborn screen interpretation (qualitative) 46741-5 Isovaleric Acidemia/2-Methylbutyric Acidemia newborn screen interpretation 46742-3 Maple syrup urine disease newborn screen interpretation 46743-1 Organic acidemias newborn screen interpretation 46744-9 Other amino acidopathies newborn screen interpretation (qualitative) 46745-6 Phenylketonuria and variants/Biopterin defects newborn screen interpretation 46746-4 Propionic/Methylmalonic Acidemias newborn screen interpretation 46747-2 Tyrosinemias newborn screen interpretation 46748-0 3-Methylcrotonic/Hydroxymethylglutaric/Methylglutaconic newborn screen interpretation (qualitative) 46749-8 2-methyl-3-hydroxybutyric Acidemias/Beta-Ketothiolase Deficiency newborn screen interpretation 46750-6 Other organic acidemias newborn screen interpretation (qualitative) 46751-4 Medium chain acyl dehydrogenase Deficiency/Glutaric Acidemia type 2 newborn screen interpretation (qualitative) 46752-2 Very long chain hydroxy acyl dehydrogenase deficiency newborn screen interpretation 46753-0 Long Chain Hydroxy Acyl Dehydrogenase/Trifunctional Protein Deficiencies newborn screen interpretation 46754-8 Carnitine uptake defect/CPT1 deficiency newborn screen interpretation (qualitative) 46755-5 Other fatty acid oxidation disorders newborn screen interpretation (qualitative) 46756-3 Congenital hypothyroidism newborn screen interpretation (qualitative) 46757-1 Congenital adrenal hyperplasia newborn screen interpretation 46758-9 Hb SS, Hb SC, Hb SB thal newborn screen interpretation (qualitative) 46759-7 Other hemoglobinopathies newborn screen interpretation (qualitative) 46760-5 Biotinidase deficiency newborn screen interpretation 46761-3 Congenital hypothyroidism newborn screen interpretation 46762-1 Secondary congenital hypothyroidism newborn screen interpretation (qualitative) 46763-9 Thyroid binding globulin deficiency newborn screen interpretation (qualitative) 46764-7 Sickle cell anemia newborn screen interpretation (qualitative) 46765-4 Hemoglobin SC disease newborn screen interpretation (qualitative) 46766-2 Hemoglobin S/Beta Thalassemia newborn screen interpretation (qualitative) 46767-0 Sickle cell carrier (trait) newborn screen interpretation (qualitative) 46768-8 Cystic fibrosis newborn screen interpretation 46769-6 Classical galactosemia newborn screen interpretation (qualitative) 46771-2 Galactokinase deficiency newborn screen interpretation (qualitative) 46772-0 Galactose epimerase deficiency newborn screen interpretation (qualitative) 46773-8 Carnitine uptake deficiency newborn screen interpretation 46774-6 Carnitine palmitoyltransferase 1 deficiency newborn screen interpretation 46775-3 CPT2/CACT newborn screen interpretation 46776-1 Glutaric acidemia 2/Ethylmalonic Encephalopathy newborn screen interpretation 46777-9