LOINCActiveObservation

LOINC Code 60588-1: t(15;17)(q24.1;q21.1)(PML,RARA) bcr2 fusion transcript Molgen Ql (Bld/Tiss)

60588-1 is a LOINC code used to identify t(15;17)(q24.1;q21.1)(PML,RARA) bcr2 fusion transcript 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(15;17)(q24.1;q21.1)(PML,RARA) bcr2 fusion transcript. 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(15;17)(q24.1;q21.1)(PML,RARA) bcr2 fusion transcript. 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: Observation
  • Method: Molgen

What it does not mean

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

Key facts

  • t(15;17)(q24.1;q21.1)(PML,RARA) bcr2 fusion transcript [Presence] in Blood or Tissue by Molecular genetics method
  • t(15;17)(q24.1;q21.1)(PML,RARA) bcr2 fusion transcript
  • Acute promyelocytic leukemia; APL; Arbitrary; Blood; breakpoint cluster region 2; DNA; gene fusion; gene translocation; Genetics; Heredity; Heritable; Inherited; Molecular genetics; Molecular pathology; MOLPATH; MOLPATH.TRANSLOCATION; Myelogenous; MYL; NR1B1; Ordinal; PCR; PML-1; PML-2; PML-3; PML-3B; PML-X; Point in time; Promyelocytic leukemia; QL; Qual; Qualitative; Random; RAR alpha form; RARalpha; Retinoic acid receptor alpha; RNA; Screen; T prime; t(15,17) (PML,RARA) gene translocation; t(15,17)(PML,RARA) gene translocation breakpoint cluster region 2; t(15,17)(q22,q11.2-q12); t(15;17) BCR2; t(15;17)(PML,RARA); 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(15;17)(q24.1;q21.1)(PML,RARA) bcr2 fusion transcript Molgen Ql (Bld/Tiss)t(15;17)(q24.1;q21.1)(PML,RARA) bcr2 fusion transcript [Presence] in Blood or Tissue by Molecular genetics methodt(15;17) BCR2 Bld/T Qlt(15;17)(q24.1;q21.1)(PML,RARA) bcr2 fusion transcriptMOLPATH.TRNLOCt(15;17)(q24.1;q21.1)(PML,RARA) Bcr2 fusion transcript analysis, Blood or tissue specimenArb

Frequently asked questions

Code details

Code60588-1
SystemLOINC
Display namet(15;17)(q24.1;q21.1)(PML,RARA) bcr2 fusion transcript Molgen Ql (Bld/Tiss)
Descriptiont(15;17)(q24.1;q21.1)(PML,RARA) bcr2 fusion transcript
Short namet(15;17) BCR2 Bld/T Ql
Componentt(15;17)(q24.1;q21.1)(PML,RARA) bcr2 fusion transcript
PropertyArb
TimingPt
System (specimen)Bld/Tiss
ScaleOrd
MethodMolgen
ClassMOLPATH.TRNLOC
StatusACTIVE
Order/ObservationObservation

Flags

BillableNo
Valid clinical useNo

Source

SourceLOINC
Version2.82
Releasemain
First released2.36
Last changed2.40

Consumer names

t(15;17)(q24.1;q21.1)(PML,RARA) Bcr2 fusion transcript analysis, Blood or tissue specimen

Part names

t(15;17)(q24.1;q21.1)(PML,RARA) bcr2 fusion transcriptArbPtBld/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.