LOINCActiveBoth

LOINC Code 21809-9: t(14;18)(q32;q21.3)(IGH,BCL2) fusion transcript major break points Molgen Ql (Bld/Tiss)

21809-9 is a LOINC code used to identify t(14;18)(q32;q21.3)(IGH,BCL2) fusion transcript major break points Molgen 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 t(14;18)(q32;q21.3)(IGH,BCL2) fusion transcript major break points. 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 t(14;18)(q32;q21.3)(IGH,BCL2) fusion transcript major break points. 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: Molgen

What it does not mean

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

Key facts

  • t(14;18)(q32;q21.3)(IGH,BCL2) fusion transcript major break points [Presence] in Blood or Tissue by Molecular genetics method
  • t(14;18)(q32;q21.3)(IGH,BCL2) fusion transcript major break points
  • Arbitrary; B-cell leukemia/lymphoma 2; B-cell NHL; B-cell non-hodgkin lymphoma; BCL-2; Blood; breakpoint; DNA; Follicular B cell lymphoma; gene fusion; gene translocation; Genetics; Heredity; Heritable; Inherited; Mbr; Molecular genetics; Molecular pathology; MOLPATH; MOLPATH.TRANSLOCATION; Ordinal; PCR; Point in time; QL; Qual; Qualitative; Random; RNA; Screen; T prime; t(14,18)(IGH,BCL2) gene translocation; t(14,18)(IGH,BCL2) gene translocation major break points; t(14;18)(IGH,BCL2); Tissue; Tissue, unspecified; translocation; 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

t(14;18)(q32;q21.3)(IGH,BCL2) fusion transcript major break points Molgen Ql (Bld/Tiss)t(14;18)(q32;q21.3)(IGH,BCL2) fusion transcript major break points [Presence] in Blood or Tissue by Molecular genetics methodt(14;18)(IGH,BCL2) Major Bld/T Qlt(14;18)(q32;q21.3)(IGH,BCL2) fusion transcript major break pointsMOLPATH.TRNLOCt(14;18)(q32;q21.3)(IGH,BCL2) major break point analysis, Blood or tissue specimenArb

Frequently asked questions

Code details

Code21809-9
SystemLOINC
Display namet(14;18)(q32;q21.3)(IGH,BCL2) fusion transcript major break points Molgen Ql (Bld/Tiss)
Descriptiont(14;18)(q32;q21.3)(IGH,BCL2) fusion transcript major break points
Short namet(14;18)(IGH,BCL2) Major Bld/T Ql
Componentt(14;18)(q32;q21.3)(IGH,BCL2) fusion transcript major break points
PropertyArb
TimingPt
System (specimen)Bld/Tiss
ScaleOrd
MethodMolgen
ClassMOLPATH.TRNLOC
StatusACTIVE
Order/ObservationBoth

Flags

BillableNo
Valid clinical useNo

Source

SourceLOINC
Version2.82
Releasemain
First released1.0m
Last changed2.50

Consumer names

t(14;18)(q32;q21.3)(IGH,BCL2) major break point analysis, Blood or tissue specimen

Part names

t(14;18)(q32;q21.3)(IGH,BCL2) fusion transcript major break pointsArbPtBld/TissOrdMolgenArbitraryPoint in time (spot)Blood or TissueMolecular genetics

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 21809-9 | HealthAssure