LOINCActiveBoth

LOINC Code 21771-1: Chr 21 trisomy Cytogenetics Ql (Bld/Tiss)

21771-1 is a LOINC code used to identify Chr 21 trisomy Cytogenetics Ql (Bld/Tiss) 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 Chromosome 21 trisomy. It is commonly used with the system or sample type Bld/Tiss.

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 Chromosome 21 trisomy. It is commonly used with the system or sample type Bld/Tiss.

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: Cytogenetics

What it does not mean

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

Key facts

  • Chromosome 21 trisomy [Presence] in Blood or Tissue by Cytogenetics
  • Chromosome 21 trisomy
  • Arbitrary; Blood; Chr 21 Ts; Chromosom; Chromosomes; Cytog; Down syndrome; Downs; Genetics; Heredity; Heritable; Inherited; Karyotype; Molecular pathology; MOLPATH; MOLPATH.TRISOMY; Ordinal; Point in time; QL; Qual; Qualitative; Random; Screen; Tissue; Tissue, unspecified; Ts; WB; Whole blood; Whole blood or Tissue

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

Chr 21 trisomy Cytogenetics Ql (Bld/Tiss)Chromosome 21 trisomy [Presence] in Blood or Tissue by CytogeneticsChr 21 Ts Bld/T QlChromosome 21 trisomyMOLPATH.TRISOMYChromosome 21 trisomy, Blood or tissue specimenArb

Frequently asked questions

Code details

Code21771-1
SystemLOINC
Display nameChr 21 trisomy Cytogenetics Ql (Bld/Tiss)
DescriptionChromosome 21 trisomy
Short nameChr 21 Ts Bld/T Ql
ComponentChromosome 21 trisomy
PropertyArb
TimingPt
System (specimen)Bld/Tiss
ScaleOrd
MethodCytogenetics
ClassMOLPATH.TRISOMY
StatusACTIVE
Order/ObservationBoth

Flags

BillableNo
Valid clinical useNo

Source

SourceLOINC
Version2.82
Releasemain
First released1.0m
Last changed2.73

Consumer names

Chromosome 21 trisomy, Blood or tissue specimen

Part names

Chromosome 21 trisomyArbPtBld/TissOrdCytogeneticsArbitraryPoint in time (spot)Blood or Tissue

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.

LOINC Code 21771-1 | HealthAssure