LOINCActiveBoth

LOINC Code 101377-0: inv(16)(p13.1;q22.1)(MYH11,CBFB) fusion transcript Molgen Doc (Bld/BM)

101377-0 is a LOINC code used to identify inv(16)(p13.1;q22.1)(MYH11,CBFB) fusion transcript Molgen Doc (Bld/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 inv(16)(p13.1;q22.1)(MYH11,CBFB) fusion transcript. It is commonly used with the system or sample type Bld/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 inv(16)(p13.1;q22.1)(MYH11,CBFB) fusion transcript. It is commonly used with the system or sample type Bld/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: Both
  • Method: Molgen

What it does not mean

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

Key facts

  • inv(16)(p13.1;q22.1)(MYH11,CBFB) fusion transcript in Blood or Marrow by Molecular genetics method
  • inv(16)(p13.1;q22.1)(MYH11,CBFB) fusion transcript
  • Acute myeloid leukemia; AML; Bld/Mar; Blood; BM; BON; Bone marrow; DNA; Document; Finding; Findings; gene fusion; gene translocation; inv(16)(CBFB,MYH11) gene inversion; inv(16)(p13;q22); Inversion 16; MAR; Marrow (bone); minimal angle of resolution; Minimum angle of resolution; Molecular genetics; Molecular pathology; MOLPATH; PCR; Point in time; Random; RNA; translocation; WB; Whole blood; Whole blood or Bone marrow

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

inv(16)(p13.1;q22.1)(MYH11,CBFB) fusion transcript Molgen Doc (Bld/BM)inv(16)(p13.1;q22.1)(MYH11,CBFB) fusion transcript in Blood or Marrow by Molecular genetics methodinv(16)(p13;q22) Bld/Marinv(16)(p13.1;q22.1)(MYH11,CBFB) fusion transcriptMOLPATHinv(16)(p13.1;q22.1)(MYH11,CBFB) fusion transcript analysis, Blood Or Bone marrowFind

Frequently asked questions

Code details

Code101377-0
SystemLOINC
Display nameinv(16)(p13.1;q22.1)(MYH11,CBFB) fusion transcript Molgen Doc (Bld/BM)
Descriptioninv(16)(p13.1;q22.1)(MYH11,CBFB) fusion transcript
Short nameinv(16)(p13;q22) Bld/Mar
Componentinv(16)(p13.1;q22.1)(MYH11,CBFB) fusion transcript
PropertyFind
TimingPt
System (specimen)Bld/Bone mar
ScaleDoc
MethodMolgen
ClassMOLPATH
StatusACTIVE
Order/ObservationBoth

Flags

BillableNo
Valid clinical useNo

Source

SourceLOINC
Version2.82
Releasemain
First released2.74
Last changed2.75

Consumer names

inv(16)(p13.1;q22.1)(MYH11,CBFB) fusion transcript analysis, Blood Or Bone marrow

Part names

inv(16)(p13.1;q22.1)(MYH11,CBFB) fusion transcriptFindPtBld/Bone marDocMolgenFindingPoint in time (spot)Blood or 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 101377-0 | HealthAssure