75979-5

LOINC Code


LOINC code75979-5
name
descriptionThe interpretation of chromosome 13 aneuploidy (e.g., consistent with diploid, suspected trisomy or consistent with trisomy 13) based on non-invasive prenatal screening methods using cfDNA in maternal plasma.
statusACTIVE

Fully-Specified Name

componentFetal chromosome 13 trisomy
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 nameChr 13 Ts; Chromosom; Chromosomes; Genetics; Heredity; Heritable; Impression; Impression/interpretation of study; Impressions; Inherited; Interp; Interpretation; Molecular pathology; MOLPATH; MOLPATH.TRISOMY; Ordinal; Pl; Plasma; Plsm; Point in time; QL;

Basic Attributes

classMOLPATH.TRISOMY
type1  Laboratory
order vs. observationFet Chr 13 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.

demo
request yours today
subscribe
start today
newsletter
free subscription

Thank you for choosing Find-A-Code, please Sign In to remove ads.

Aimee - AI-powered coding assistant Would you like Aimee - AI
to help you with this?