t(9;22)(q34.1;q11)(ABL1,BCR) b2a2 fusion transcript [Presence] in Blood or Tissue by Molecular genetics method   75015-8

LOINC Code


LOINC code75015-8
namet(9;22)(q34.1;q11)(ABL1,BCR) b2a2 fusion transcript [Presence] in Blood or Tissue by Molecular genetics method
statusACTIVE

Fully-Specified Name

componentt(9;22)(q34.1;q11)(ABL1,BCR) b2a2 fusion transcript
propertyPrThr  =  Present or threshold:  The Property PrThr stands for “Presence or Threshold”, meaning either a) the actual presence or absence of an analyte, or b) that the amount of analyte detected is over some predetermined threshold.
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
scaleOrd  =  Ordinal:  Ordered categorical responses, e.g., 1+, 2+, 3+; positive, negative; reactive, indeterminate, nonreactive.
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(ABL1,BCR)b2a2 Bld/T Ql

Basic Attributes

classMOLPATH
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

first released
last updated2.56
last change typeMIN  - change to field other than name
change reasonThe PrThr property is used for LOINC terms whose results are reported using an ordered categorical scale, regardless of whether or not an internal threshold was used to make that determination. This change was approved by the Laboratory LOINC Committee in June 2016.

Related Names

ABL
ALL
bcr/abl
BCR1
bcr-abl1
Blood
Breakpoint cluster region
Chronic myeloid leukemia
CML
D22S11
D22S662
DNA
gene fusion
gene translocation
Genetics
Heredity
Heritable
Inherited
JTK7
major breakpoints
Mbr
Mcr
minor breakpoints
Molecular genetics
Molecular pathology
MOLPATH
Ordinal
p150
PCR
Ph chromosome
Philadelphia chromosome
PHL
Point in time
PR
QL
Qual
Qualitative
Random
RNA
Screen
T prime
t(9,22)(ABL1,BCR) gene translocation
t(9,22)(ABL1,BCR) p210 gene translocation
t(9,22)(ABL1,BCR) Translocation
t(9,22)(q34,q11)
t(9,22)(q34.1,q11)
t(9
22)(ABL1,BCR)
t(ABL1,BCR)b2a2
Tissue
Tissue, unspecified
translocation
v-abl Abelson murine leukemia viral oncogene homolog 1
WB
Whole blood
Whole blood or Tissue

Copyright © 2024 Regenstrief Institute, Inc. All Rights Reserved. To the extent included herein, the LOINC table and LOINC codes are copyright © 1995-2024, 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.