LOINC Home

{component}   LP432695-7

Laboratory   LP29693-6

Molecular pathology   LP7822-2

Genetic screen   LP19405-7

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.

▸ Cell-free DNA.fetal   LP185863-0

▸ Genetic screen | XXX | Molecular pathology   LP401840-6

▸ Cell-free DNA.donor   LP430954-0

▸ Fetal microdeletions risk   LP200456-4

▸ Fetal Angelman syndrome risk   LP185771-5

▸ Angelman syndrome prior risk   LP185772-3

▸ Comment on fetal Angelman syndrome risk   LP185991-9

▸ Fetal monosomy X risk   LP185775-6

▸ Monosomy X prior risk   LP185767-3

▸ Comment on fetal Monosomy X risk   LP185988-5

▸ Comment on overall fetal aneuploidy risk   LP422368-3

▸ Fetal sex   LP410743-1

▸ Hepatocellular carcinoma screening   LP430692-6

▸ Noninvasive prenatal testing overall interpretation   LP428616-9

▸ Deletions   LP7823-0

▸ Trisomies   LP7827-1


Copyright © 2024 Regenstrief Institute, Inc. All Rights Reserved. To the extent included herein, the LOINC table and LOINC codes are copyright © 1995-2024, 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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