LOINCActiveBoth

LOINC Code 81873-2: Xp22.33 AndOr Yp11.32 del and dup mutation analysis MLPA Doc (Bld/Tiss)

81873-2 is a LOINC code used to identify Xp22.33 AndOr Yp11.32 del and dup mutation analysis MLPA Doc (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 region Xp22.33 &or Yp11.32 deletion+duplication. 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 region Xp22.33 &or Yp11.32 deletion+duplication. 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: MLPA

What it does not mean

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

Key facts

  • Chromosome region Xp22.33 AndOr Yp11.32 deletion and duplication mutation analysis in Blood or Tissue by MLPA
  • Chromosome region Xp22.33 &or Yp11.32 deletion+duplication
  • Detection of deletions or duplications in the Xp22.33 and Yp11.32 regions of the sex chromosomes, which contain the pseudoautosomal region 1 (PAR1) and SHOX gene, by MLPA analysis. This term was created for, but not limited in use to, the submitter's kit, SALSA MLPA P018 SHOX probemix.
  • Amplification; Blood; Chr Xp22.33 +or Yp11.32 deletion+duplication; Chromosom; Chromosomes; Cyto loc; Del; Del+Dup; Deletions; Document; Dp; Finding; Findings; Genetics; Heredity; Heritable; Inherited; Molecular pathology; MOLPATH; MOLPATH.DELDUP; Point in time; Random; SHOX; Tissue; Tissue, unspecified; WB; Whole blood; Whole blood or Tissue; Xp22.33 +or Yp11.32

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

Xp22.33 AndOr Yp11.32 del and dup mutation analysis MLPA Doc (Bld/Tiss)Chromosome region Xp22.33 AndOr Yp11.32 deletion and duplication mutation analysis in Blood or Tissue by MLPAXp22.33 +or Yp11.32 Del+Dup Bld/T MLPAChromosome region Xp22.33 &or Yp11.32 deletion+duplicationMOLPATH.DELDUPXp22.33 andOr Yp11.32 deletion/duplication analysis, Blood or tissue specimenFind

Frequently asked questions

Code details

Code81873-2
SystemLOINC
Display nameXp22.33 AndOr Yp11.32 del and dup mutation analysis MLPA Doc (Bld/Tiss)
DescriptionChromosome region Xp22.33 &or Yp11.32 deletion+duplication
Short nameXp22.33 +or Yp11.32 Del+Dup Bld/T MLPA
ComponentChromosome region Xp22.33 &or Yp11.32 deletion+duplication
PropertyFind
TimingPt
System (specimen)Bld/Tiss
ScaleDoc
MethodMLPA
ClassMOLPATH.DELDUP
StatusACTIVE
Order/ObservationBoth

Flags

BillableNo
Valid clinical useNo

Source

SourceLOINC
Version2.82
Releasemain
First released2.56
Last changed2.65

Consumer names

Xp22.33 andOr Yp11.32 deletion/duplication analysis, Blood or tissue specimen

Part names

Chromosome region Xp22.33 &or Yp11.32 deletion+duplicationFindPtBld/TissDocMLPAChromosome region Xp22.33 AndOr Yp11.32 deletion+duplicationFindingPoint 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.