75983-7

LOINC Code


LOINC code75983-7
name
descriptionIndicates the presence of trisomy 21 in the fetus based on non-invasive prenatal screening methods using cfDNA from maternal plasma.
statusACTIVE

Fully-Specified Name

componentFetal chromosome 21 trisomy
propertyPrThr  =  Present or threshold:  The Property PrThr stands for “Presence or Threshold”, meaning either a) the actual presence or absence of an analyte, or b) that the amount of analyte detected is over some predetermined threshold.
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 nameChr 21 Ts; Chromosom; Chromosomes; Down syndrome; Downs; Genetics; Heredity; Heritable; Inherited; Molecular pathology; MOLPATH; MOLPATH.TRISOMY; Ordinal; Pl; Plasma; Plsm; Point in time; PR; QL; Qual; Qualitative; Random; Screen; Spec; Ts

Basic Attributes

classMOLPATH.TRISOMY
type1  Laboratory
order vs. observationFet Chr 21 Ts P

History/Usage

first released
last updated2.73
last change typeMIN  - change to field other than name

Related Names



Copyright © 2026 Regenstrief Institute, Inc. All Rights Reserved. To the extent included herein, the LOINC table and LOINC codes are copyright © 1995-2026, 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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