LOINCBoth

LOINC Code 81750-2: t(9;22)(q34.1;q11)(ABL1,BCR) fusion transcript Molgen Doc (BM)

81750-2 is a LOINC code used to identify t(9;22)(q34.1;q11)(ABL1,BCR) fusion transcript Molgen Doc (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(9;22)(q34.1;q11)(ABL1,BCR) fusion transcript. 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(9;22)(q34.1;q11)(ABL1,BCR) fusion transcript. 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: DEPRECATED
  • Order vs observation: Both
  • Method: Molgen

What it does not mean

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

Key facts

  • Deprecated t(9;22)(q34.1;q11)(ABL1,BCR) fusion transcript in Bone marrow by Molecular genetics method
  • t(9;22)(q34.1;q11)(ABL1,BCR) fusion transcript
  • ABL; ALL; bcr/abl; BCR1; bcr-abl1; BM; BON; Bone marrow; Breakpoint cluster region; Chronic myeloid leukemia; CML; D22S11; D22S662; DNA; Document; Finding; Findings; gene fusion; gene translocation; Genetics; Heredity; Heritable; Inherited; JTK7; major breakpoints; MAR; Marrow (bone); Mbr; Mcr; minimal angle of resolution; Minimum angle of resolution; minor breakpoints; Molecular genetics; Molecular pathology; MOLPATH; MOLPATH.TRANSLOCATION; p150; PCR; Ph chromosome; Philadelphia chromosome; PHL; Point in time; Random; RNA; T prime; t(9,22)(ABL1,BCR) gene translocation; t(9,22)(ABL1,BCR) Translocation; t(9,22)(q34,q11); t(9,22)(q34.1,q11); t(9;22)(ABL1,BCR); translocation; v-abl Abelson murine leukemia viral oncogene homolog 1

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(9;22)(q34.1;q11)(ABL1,BCR) fusion transcript Molgen Doc (BM)Deprecated t(9;22)(q34.1;q11)(ABL1,BCR) fusion transcript in Bone marrow by Molecular genetics methodDeprecated t(9;22)(ABL1,BCR) Mart(9;22)(q34.1;q11)(ABL1,BCR) fusion transcriptMOLPATH.TRNLOCt(9;22)(q34.1;q11)(ABL1,BCR) fusion transcript analysis, Bone marrowFind

Frequently asked questions

Code details

Code81750-2
SystemLOINC
Display namet(9;22)(q34.1;q11)(ABL1,BCR) fusion transcript Molgen Doc (BM)
Descriptiont(9;22)(q34.1;q11)(ABL1,BCR) fusion transcript
Short nameDeprecated t(9;22)(ABL1,BCR) Mar
Componentt(9;22)(q34.1;q11)(ABL1,BCR) fusion transcript
PropertyFind
TimingPt
System (specimen)Bone mar
ScaleDoc
MethodMolgen
ClassMOLPATH.TRNLOC
StatusDEPRECATED
Order/ObservationBoth

Flags

BillableNo
Valid clinical useNo

Source

SourceLOINC
Version2.82
Releasemain
First released2.56
Last changed2.66

Consumer names

t(9;22)(q34.1;q11)(ABL1,BCR) fusion transcript analysis, Bone marrow

Part names

t(9;22)(q34.1;q11)(ABL1,BCR) fusion transcriptFindPtBone marDocMolgenFindingPoint 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 81750-2 | HealthAssure