LOINC Home

{component}   LP432695-7

Laboratory   LP29693-6

Lab terms not yet categorized   LP248770-2

t(9;22)(q34.1;q11)(ABL1,BCR) fusion transcript in Blood or Tissue by Molecular genetics method   50014-0

LOINC Code


LOINC code50014-0
namet(9;22)(q34.1;q11)(ABL1,BCR) fusion transcript in Blood or Tissue by Molecular genetics method
statusACTIVE

Fully-Specified Name

componentt(9;22)(q34.1;q11)(ABL1,BCR) fusion transcript
propertyFind  =  Finding
timePt  =  Point in time:  To identify measures at a point in time. This is a synonym for “spot” or “random” as applied to urine measurements.
systemBld/Tiss
    Bld  =  Whole blood
    Tiss  =  Tissue, unspecified
scaleDoc  =  Document:  A document that could be in many formats (XML, narrative, etc.)
methodMolgen  =  Molecular Genetics:  General class of methods used to detect genetic attributes on a molecular basis including RFL, PCR and other methods.

Additional Names

short namet(9;22)(ABL1,BCR) Bld/T

Basic Attributes

classMOLPATH.TRNLOC
type1  Laboratory
order vs. observationBoth

Associated Observations

LOINC codes that represent optional associated observation(s) for a clinical observation or laboratory test. A LOINC term may represent a single associated observation or panel containing several associated observations.

History/Usage

test rank7758 of 2000 most commonly performed tests by labs in USA
first released
last updated2.73
last change typeMIN  - change to field other than name
change reasonBased on review of the original submission for this term and to harmonize with current LOINC nomenclature, the Component was change from BCR-ABL to t(9;22)(q34.1;q11)(ABL1,BCR) fusion transcript.; Based on LOINC Committee review (June 2019), updated the Property from "Prid" to "Find" and Scale from "Nar" to "Doc" to align with the current LOINC model for naming collections of information reported in narrative and/or structured formats.

Related Names

ABL
ALL
bcr/abl
BCR1
bcr-abl1
Blood
Breakpoint cluster region
Chronic myeloid leukemia
CML
D22S11
D22S662
DNA
Document
Finding
Findings
gene fusion
gene translocation
Genetics
Heredity
Heritable
Inherited
JTK7
major breakpoints
Mbr
Mcr
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)
Tissue
Tissue, unspecified
translocation
v-abl Abelson murine leukemia viral oncogene homolog 1
WB
Whole blood
Whole blood or Tissue

Copyright © 2023 Regenstrief Institute, Inc. All Rights Reserved. To the extent included herein, the LOINC table and LOINC codes are copyright © 1995-2023, Regenstrief Institute, Inc. and the Logical Observation Identifiers Names and Codes (LOINC) Committee. See https://loinc.org/license for the full LOINC copyright and license.

demo
request yours today
 subscribe
start today
 newsletter
free subscription

Thank you for choosing Find-A-Code, please Sign In to remove ads.