Noninvasive prenatal fetal aneuploidy and 22q11.2 deletion panel - Plasma cell-free+WBC DNA by Dosage of chromosome-specific cfDNA   96978-2

LOINC Code


LOINC code96978-2
nameNoninvasive prenatal fetal aneuploidy and 22q11.2 deletion panel - Plasma cell-free+WBC DNA by Dosage of chromosome-specific cfDNA
descriptionThis panel includes quantitative and qualitative risk terms for aneuploidies, including trisomy 13, 18 and 21, monosomy X, and triploidy, as well as the 22q11.2 microdeletion. Noninvasive prenatal screening is used to assess fetal risk for various genetic conditions without requiring invasive maternal procedures such as amniocentesis or chorionic villus sampling. Cell-free DNA (cfDNA) in maternal plasma comes from both fetal and maternal sources, and depending on the technology used, this DNA can be used to determine fetal risk for a variety of conditions including aneuploidy (e.g., trisomy 21, monosomy X) and microdeletions (e.g., 22q11.2 deletion). This panel was developed for, but is not limited in use to, Natera's Panorama aneuploidy + 22q11.2 deletion prenatal test, which incorporates SNP analysis of maternal white blood cell DNA with combined maternal and fetal cfDNA SNP analysis. Natera's proprietary informatics analysis method (NATUS) effectively subtracts the maternal genotype from the cfDNA genotype and analyzes the remaining fetal cfDNA genotype for certain aneuploidies and microdeletion syndromes.
statusACTIVE

Fully-Specified Name

componentNoninvasive prenatal fetal aneuploidy & 22q11.2 deletion panel
property-
timePt  =  Point in time:  To identify measures at a point in time. This is a synonym for “spot” or “random” as applied to urine measurements.
systemWBC.DNA+Plas.cfDNA
scale-
methodDosage of chromosome specific cf DNA

Additional Names

short nameNIP aneu + 22q11.2 Pnl WBC.DNA+cfDNA

Basic Attributes

classPANEL.MOLPATH
type1  Laboratory
order vs. observationOrder

Associated Observations

LOINC codes that represent optional associated observation(s) for a clinical observation or laboratory test. A LOINC term may represent a single associated observation or panel containing several associated observations.

History/Usage

first released
last updated2.70
last change typeADD  - added

Related Names

Chromosom
Chromosomes
Gyn
Gynecology
Leukocytes
Molecular pathology
MOLPATH
NIP aneu + 22q11.2 Pnl
OB
ObGyn
Obstetrics
Pan
Panel.molpath
Panl
Pl
Plasma
Plsm
Pnl
Point in time
Random
Spec
WBC.DNA+cfDNA
WBCs
White blood cells

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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