LOINCActiveBoth

LOINC Code 87436-2: Chr X and Y aneuploidy FISH Doc (Bld/Tiss)

87436-2 is a LOINC code used to identify Chr X and Y aneuploidy FISH 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 X & Y aneuploidy. 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 X & Y aneuploidy. 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: FISH

What it does not mean

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

Key facts

  • Chromosome X and Y aneuploidy in Blood or Tissue by FISH
  • Chromosome X & Y aneuploidy
  • Sex chromosome (X & Y) analysis by FISH to determine gender (XY or XX) or presence of aneuploidy in blood or tissue-type specimens, including cheek (buccal) swabs or saliva. For aneuploidy cases, the results of the specific findings (e.g. YY, XYY, XXX, etc.) are reported as well. This document may contain the reason for referral, the specimen source, the overall result (normal/abnormal), the result in ISCN expression (e.g. nuc ish(DXZ1x2)[200]), the interpretation or findings, recommendations, and test method information.
  • Blood; Chr X + Y aneup; Chromosom; Chromosomes; Document; Finding; Findings; Fluorescent in situ hybridization; Genetics; Heredity; Heritable; Inherited; Molecular pathology; MOLPATH; Point in time; Random; Tissue; Tissue, unspecified; 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 X and Y aneuploidy FISH Doc (Bld/Tiss)Chromosome X and Y aneuploidy in Blood or Tissue by FISHChr X + Y aneup Bld/T FISHChromosome X & Y aneuploidyMOLPATHChromosome X and Y Aneuploidy, Blood or tissue specimenFind

Frequently asked questions

Code details

Code87436-2
SystemLOINC
Display nameChr X and Y aneuploidy FISH Doc (Bld/Tiss)
DescriptionChromosome X & Y aneuploidy
Short nameChr X + Y aneup Bld/T FISH
ComponentChromosome X & Y aneuploidy
PropertyFind
TimingPt
System (specimen)Bld/Tiss
ScaleDoc
MethodFISH
ClassMOLPATH
StatusACTIVE
Order/ObservationBoth

Flags

BillableNo
Valid clinical useNo

Source

SourceLOINC
Version2.82
Releasemain
First released2.63
Last changed2.66

Consumer names

Chromosome X and Y Aneuploidy, Blood or tissue specimen

Part names

Chromosome X & Y aneuploidyFindPtBld/TissDocFISHChromosome X and Y aneuploidyFindingPoint in time (spot)Blood or TissueFluorescent in situ hybridization (FISH)

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 87436-2 | HealthAssure