bloodwork
LOINC parts

72,372 parts · page 1236 of 1,448 · all codes

PartNameTypeTests
LP450645-9 Rehabilitation progress note COMPONENT 1
LP450669-9 Warm absorption METHOD 1
LP450671-5 Cold absorption METHOD 1
LP450681-4 ristocetin+Control PPP induced METHOD 1
LP56733-6 Francisella tularensis subtype COMPONENT 1
LP56734-4 Amino acidemias COMPONENT 1
LP56735-1 Citrullinemias/Arginosuccinic aciduria COMPONENT 1
LP56737-7 Endocrine disorders COMPONENT 1
LP56738-5 Fatty acid oxidation defects COMPONENT 1
LP56739-3 Galactosemias COMPONENT 1
LP56740-1 Genetic.Disorders COMPONENT 1
LP56741-9 Glutaric acidemia type 1 COMPONENT 1
LP56743-5 Homocystinuria and/or other hypermethioninemias COMPONENT 1
LP56744-3 Isovaleric Acidemia/2-Methylbutyric Acidemia COMPONENT 1
LP56746-8 Maple syrup urine disease COMPONENT 1
LP56747-6 Organic acidemias COMPONENT 1
LP56748-4 Other amino acidopathies COMPONENT 1
LP56749-2 Phenylketonuria and variants/Biopterin defects COMPONENT 1
LP56751-8 Propionic/Methylmalonic Acidemias COMPONENT 1
LP56753-4 Tyrosinemias COMPONENT 1
LP56754-2 3-Methylcrotonic/Hydroxymethylglutaric/Methylglutaconic COMPONENT 1
LP56756-7 2-methyl-3-hydroxybutyric Acidemias/Beta-Ketothiolase Deficiency COMPONENT 1
LP56757-5 Other organic acidemias COMPONENT 1
LP56758-3 Medium chain acyl dehydrogenase Deficiency/Glutaric Acidemia type 2 COMPONENT 1
LP56759-1 Glutaric acidemia type 2 COMPONENT
LP56760-9 Very long chain hydroxy acyl dehydrogenase deficiency COMPONENT 1
LP56761-7 Long Chain Hydroxy Acyl Dehydrogenase/Trifunctional Protein Deficiencies COMPONENT 1
LP56763-3 Carnitine uptake defect/CPT1 deficiency COMPONENT 1
LP56764-1 CPT1 deficiency COMPONENT
LP56765-8 Other fatty acid oxidation disorders COMPONENT 1
LP56766-6 Congenital hypothyroidism COMPONENT 2
LP56767-4 Congenital adrenal hyperplasia COMPONENT 1
LP56768-2 Hb SS, Hb SC, Hb SB thal COMPONENT 1
LP56770-8 Other hemoglobinopathies COMPONENT 1
LP56771-6 Biotinidase deficiency COMPONENT 1
LP56773-2 Secondary congenital hypothyroidism COMPONENT 1
LP56774-0 Thyroid binding globulin deficiency COMPONENT 1
LP56775-7 Sickle cell anemia COMPONENT 1
LP56776-5 Hemoglobin SC disease COMPONENT 1
LP56777-3 Hemoglobin S/Beta Thalassemia COMPONENT 1
LP56778-1 Sickle cell carrier (trait) COMPONENT 1
LP56779-9 Cystic fibrosis COMPONENT 1
LP56780-7 Hearing loss COMPONENT 1
LP56781-5 Classical galactosemia COMPONENT 1
LP56782-3 Galactokinase deficiency COMPONENT 1
LP56783-1 Galactose epimerase deficiency COMPONENT 1
LP56784-9 Carnitine uptake deficiency COMPONENT 1
LP56785-6 Carnitine palmitoyltransferase 1 deficiency COMPONENT 1
LP56788-0 Glutaric acidemia 2/Ethylmalonic Encephalopathy COMPONENT 1
LP56790-6 MCAD COMPONENT 1

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