Molecular pathology LP7822-2
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.
▸ Genetics results LP70194-3
▸ Mitochondria whole genome analysis LP433528-9
▸ Genes LP32747-5
▸ Ploidy LP32748-3
▸ Multigene studies LP427513-9
▸ Chromosome LP32750-9
▸ Genetic screen LP19405-7
▸ Microsatellite instability LP36464-3
▸ Karyotype LP28493-2
▸ Maternal cell contamination LP33231-9
▸ GenBank sequence accession number LP262418-9
▸ X linked heterotaxy LP62894-8
▸ Cancer risk assessment LP192128-9
▸ Identity testing LP76336-4
▸ Heart transplant acute cellular rejection risk LP200197-4
▸ Kidney transplant acute cellular rejection risk LP433666-7
▸ Platelet disorders multigene analysis LP433075-1
▸ Zygosity LP94227-3
▸ Prostate cancer multigene analysis LP432157-8
▸ Plasma cell proliferation analysis LP426512-2
▸ SMN1 gene silent carrier analysis LP432502-5
▸ Tripartite motif containing 46 LP437480-9
▸ Pharmacogenomics LP202929-8
▸ Copy number variation analysis LP433611-3
▸ Molecular Pathology Panels LP62072-1
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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