LOINCActiveObservation

LOINC Code 49793-3: t(14;18)(q32;q21.3)(IGH,BCL2) fusion transcript major break points Molgen Ql (BM)

49793-3 is a LOINC code used to identify t(14;18)(q32;q21.3)(IGH,BCL2) fusion transcript major break points Molgen Ql (BM) 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 Bone mar.

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 Bone mar.

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: Observation
  • 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 Bone marrow 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; BM; BON; Bone marrow; breakpoint; DNA; Follicular B cell lymphoma; gene fusion; gene translocation; Genetics; Heredity; Heritable; Inherited; MAR; Marrow (bone); Mbr; minimal angle of resolution; Minimum angle of resolution; 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); translocation

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 (BM)t(14;18)(q32;q21.3)(IGH,BCL2) fusion transcript major break points [Presence] in Bone marrow by Molecular genetics methodt(14;18)(IGH,BCL2) Major Mar 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, Bone marrowArb

Frequently asked questions

Code details

Code49793-3
SystemLOINC
Display namet(14;18)(q32;q21.3)(IGH,BCL2) fusion transcript major break points Molgen Ql (BM)
Descriptiont(14;18)(q32;q21.3)(IGH,BCL2) fusion transcript major break points
Short namet(14;18)(IGH,BCL2) Major Mar Ql
Componentt(14;18)(q32;q21.3)(IGH,BCL2) fusion transcript major break points
PropertyArb
TimingPt
System (specimen)Bone mar
ScaleOrd
MethodMolgen
ClassMOLPATH.TRNLOC
StatusACTIVE
Order/ObservationObservation

Flags

BillableNo
Valid clinical useNo

Source

SourceLOINC
Version2.82
Releasemain
First released2.22
Last changed2.50

Consumer names

t(14;18)(q32;q21.3)(IGH,BCL2) major break point analysis, Bone marrow

Part names

t(14;18)(q32;q21.3)(IGH,BCL2) fusion transcript major break pointsArbPtBone marOrdMolgenArbitraryPoint in time (spot)Bone marrowMolecular 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 49793-3 | HealthAssure