What does this LOINC code represent?

This LOINC code identifies a lab observation, measurement, question, or clinical concept in a standardized format.

Is this enough to understand my test result?

No. The code identifies the test or observation, but the interpretation depends on the actual result, reference range, and clinical context.

LOINCActiveBoth

LOINC Code 111735-7: Chromosomal aneuploidy likelihood analysis NIPS Doc (cfDNA)

Name: LOINC Code 111735-7: Chromosomal aneuploidy likelihood analysis NIPS Doc (cfDNA)
Creator: HealthAssure Clinical Team
Published: 2026-05-21T11:17:21.942Z

111735-7 is a LOINC code used to identify Chromosomal aneuploidy likelihood analysis NIPS Doc (cfDNA) in laboratory and clinical observation data. You may see this code in lab systems, lab reports, EHR exports, interoperability feeds, or other structured clinical data exchanges. LOINC codes identify tests, measurements, observations, survey items, and clinical questions in a standardized way. It is associated with the component Chromosomal aneuploidy likelihood analysis. It is commonly used with the system or sample type Plas.cfDNA.

Reviewed by HealthAssure Clinical TeamUpdated 21 May 2026

What is this code?

LOINC codes identify tests, measurements, observations, survey items, and clinical questions in a standardized way. It is associated with the component Chromosomal aneuploidy likelihood analysis. It is commonly used with the system or sample type Plas.cfDNA.

When is it used?

Used in lab systems, EHRs, and clinical data exchange.
May identify a test, observation, survey item, or clinical document request rather than a diagnosis.
Status: ACTIVE
Order vs observation: Both
Method: NIPS

What it does not mean

The code identifies the observation or test, not the actual result.

Key facts

Chromosomal aneuploidy likelihood analysis in Plasma cell-free DNA by NIPS

Chromosomal aneuploidy likelihood analysis

This term represents indicates the presence of an aneuploidy involving chromosome 13, 18, 21, X, or Y in the fetus, as determined by noninvasive prenatal screening (NIPS) using cell-free DNA (cfDNA) analysis of maternal plasma. The result reflects detection of any such aneuploidy, but does not specify which particular chromosome abnormality is present if an abnormal result is reported. [PMID24466384]

Document; Finding; Findings; Molecular pathology; MOLPATH; MOLPATH.TRISOMY; Pl; Plasma; Plsm; Point in time; Random; Ts

Where you may see this code

You may see this code in lab systems, lab reports, EHR exports, interoperability feeds, or other structured clinical data exchanges.

Common synonyms

Chromosomal aneuploidy likelihood analysis NIPS Doc (cfDNA)Chromosomal aneuploidy likelihood analysis in Plasma cell-free DNA by NIPSChromosomal aneuploidy likelihood analysis Plas.cfDNA NIPSChromosomal aneuploidy likelihood analysisMOLPATH.TRISOMYFetal Chromosomal aneuploidy likelihood analysisFind

Frequently asked questions

Code details

Code111735-7

SystemLOINC

Display nameChromosomal aneuploidy likelihood analysis NIPS Doc (cfDNA)

DescriptionChromosomal aneuploidy likelihood analysis

Short nameChromosomal aneuploidy likelihood analysis Plas.cfDNA NIPS

ComponentChromosomal aneuploidy likelihood analysis

PropertyFind

TimingPt

System (specimen)Plas.cfDNA

ScaleDoc

MethodNIPS

ClassMOLPATH.TRISOMY

StatusACTIVE

Order/ObservationBoth

Flags

BillableNo

Valid clinical useNo

Source

SourceLOINC

Version2.82

Releasemain

First released2.82

Last changed2.82

Consumer names

Fetal Chromosomal aneuploidy likelihood analysis

Part names

Chromosomal aneuploidy likelihood analysisFindPtPlas.cfDNADocNIPSFindingPoint in time (spot)Plasma cell-free DNA

About this content

This page is prepared by HealthAssure's clinical team using official coding standards from LOINC. AI tools assist with drafting explanations, which are then reviewed and verified by healthcare professionals for accuracy. This content is for informational purposes and does not replace professional medical advice. Meet our team.