LOINCActiveObservation

LOINC Code 60576-6: t(14;18)(q32;q21.3)(IGH,BCL2) fusion transcript major break points Molgen Ql (CSF)

60576-6 is a LOINC code used to identify t(14;18)(q32;q21.3)(IGH,BCL2) fusion transcript major break points Molgen Ql (CSF) 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 CSF.

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 CSF.

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 Cerebral spinal fluid 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; breakpoint; Cerebral spinal fluid; Cerebrospinal Fl; DNA; Follicular B cell lymphoma; gene fusion; gene translocation; Genetics; Heredity; Heritable; Inherited; Mbr; Molecular genetics; Molecular pathology; MOLPATH; MOLPATH.TRANSLOCATION; Neuro; Neurology; Ordinal; PCR; Point in time; QL; Qual; Qualitative; Random; RNA; Screen; Spinal Fl; Spinal Fld; Spinal Flu; Spinal Fluid; 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 (CSF)t(14;18)(q32;q21.3)(IGH,BCL2) fusion transcript major break points [Presence] in Cerebral spinal fluid by Molecular genetics methodt(14;18)(IGH,BCL2) Major CSF 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, Spinal fluidArb

Frequently asked questions

Code details

Code60576-6
SystemLOINC
Display namet(14;18)(q32;q21.3)(IGH,BCL2) fusion transcript major break points Molgen Ql (CSF)
Descriptiont(14;18)(q32;q21.3)(IGH,BCL2) fusion transcript major break points
Short namet(14;18)(IGH,BCL2) Major CSF Ql
Componentt(14;18)(q32;q21.3)(IGH,BCL2) fusion transcript major break points
PropertyArb
TimingPt
System (specimen)CSF
ScaleOrd
MethodMolgen
ClassMOLPATH.TRNLOC
StatusACTIVE
Order/ObservationObservation

Flags

BillableNo
Valid clinical useNo

Source

SourceLOINC
Version2.82
Releasemain
First released2.38
Last changed2.50

Consumer names

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

Part names

t(14;18)(q32;q21.3)(IGH,BCL2) fusion transcript major break pointsArbPtCSFOrdMolgenArbitraryPoint in time (spot)Cerebral spinal fluidMolecular 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 60576-6 | HealthAssure