Fetal 22q11.2 deletion risk [Interpretation] based on Plasma cell-free DNA by Dosage of chromosome-specific cfDNA Qualitative   88572-3

LOINC Code


LOINC code88572-3
nameFetal 22q11.2 deletion risk [Interpretation] based on Plasma cell-free DNA by Dosage of chromosome-specific cfDNA Qualitative
descriptionThe ordinal risk interpretation (e.g. high risk/low risk or high probability/low probability) of the fetus having a 22q11.2 deletion based on dosage of chromosome specific cell-free DNA (cf DNA) in maternal plasma that contains both fetal and maternal DNA. Results may also be based on the mother's current age, IVF status (self, non-self, or not applicable), and gestational age. This code is based, but not limited in use to, the submitter's test, the Harmony Prenatal Test, a non-invasive prenatal test for screening of fetal aneuploidy as well as the 22q11.2 deletion.
statusACTIVE

Fully-Specified Name

componentFetal 22q11.2 deletion risk
propertyImp  =  Impression/interpretation of study
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.
systemPlas.cfDNA
scaleOrd  =  Ordinal:  Ordered categorical responses, e.g., 1+, 2+, 3+; positive, negative; reactive, indeterminate, nonreactive.
methodDosage of chromosome specific cf DNA

Additional Names

short nameFet 22q11.2 del risk Plas.cfDNA Ql

Basic Attributes

classMOLPATH.DELDUP
type1  Laboratory
order vs. observationObservation

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.

Member of these Panels

73967-2Noninvasive prenatal fetal aneuploidy panel - Plasma cell-free DNA

History/Usage

first released
last updated2.66
last change typeNAM  - change to Analyte/Component
change reasonAdded "Fetal" to Component to clarify that the result is about the fetus.

Related Names

22q11.2 del risk
Chromosom
Chromosomes
Genetics
Heredity
Heritable
Impression
Impression/interpretation of study
Impressions
Inherited
Interp
Interpretation
Molecular pathology
MOLPATH
MOLPATH.DELDUP
Ordinal
Pl
Plasma
Plsm
Point in time
QL
Qual
Qualitative
Random
Screen
Spec

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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