LOINC Home

{component}   LP432695-7

Laboratory   LP29693-6

Molecular pathology   LP7822-2

Molecular Pathology Panels   LP62072-1

LOINC Hierarchy


Select the title to see children of the section (▸) or the LOINC code. Select a code to view information about the section/code.

▸ Abnormal hemoglobin gene panel   LP94307-3

▸ Acute and chronic leukemia fusion transcript panel   LP156442-8

▸ Acute and chronic leukemia fusion transcript per control transcript panel   LP156443-6

▸ Alpha globin gene deletion panel   LP433648-5

▸ Alpha thalassemia gene panel   LP94306-5

▸ Breast cancer 10-year risk of distant recurrence panel   LP188517-9

▸ Chromosome analysis basic associated observations panel   LP190674-4

▸ Clinical genetic report summary panel   LP65485-2

▸ Complex variant panel   LP212294-5

▸ DNA analysis discrete sequence variation basic associated observations panel   LP190673-6

▸ F2 gene.c.20210G>A and c.1691G>A panel   LP417219-5

▸ Genechip kit panel   LP62074-7

▸ Haplotype definition panel   LP232214-9

▸ ERBB2 gene (HER2) duplication associated observations panel   LP183636-2

▸ HL7 cytogenetics panels   LP111373-9

▸ HTT gene mutation panel   LP71244-5

▸ KIR genotyping panel   LP116662-0

▸ Master HL7 genetic variant reporting panel   LP212290-3

▸ Medication usage implications panel   LP213618-4

▸ Monotypic plasma cell identification and risk stratification panel   LP410828-0

▸ Noninvasive prenatal fetal 13 and 18 and 21 aneuploidy panel   LP189736-4

▸ Noninvasive prenatal fetal 18 and 21 aneuploidy panel   LP189735-6

▸ Noninvasive prenatal fetal aneuploidy and 22q11.2 deletion panel   LP422145-5

▸ Noninvasive prenatal fetal aneuploidy and microdeletion panel   LP185919-0

▸ Noninvasive prenatal fetal aneuploidy panel   LP173436-9

▸ Pharmacogenomic analysis basic associated observations panel   LP199197-7

▸ Pharmacogenomics result panel   LP213619-2

▸ Sequence variation panel   LP62071-3

▸ Sequencing methodology panel   LP62075-4

▸ Metagenomic DNA and RNA Sequencing   LP437401-5

▸ Simple variant panel   LP212293-7

▸ Spinal muscular atrophy newborn screening panel   LP288643-2

▸ Structural variant panel   LP212396-8

▸ t(9;22)(q34.1;q11)(ABL1,BCR) transcript detection panel   LP68320-8


Copyright © 2023 Regenstrief Institute, Inc. All Rights Reserved. To the extent included herein, the LOINC table and LOINC codes are copyright © 1995-2023, Regenstrief Institute, Inc. and the Logical Observation Identifiers Names and Codes (LOINC) Committee. See https://loinc.org/license for the full LOINC copyright and license.

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