t(9;22)(q34.1;q11)(ABL1,BCR) e1a2 fusion transcript/control transcript [# Ratio] in Blood or Tissue by Molecular genetics method   52132-8

LOINC Code


LOINC code52132-8
namet(9;22)(q34.1;q11)(ABL1,BCR) e1a2 fusion transcript/control transcript [# Ratio] in Blood or Tissue by Molecular genetics method
statusACTIVE

Fully-Specified Name

componentt(9;22)(q34.1;q11)(ABL1,BCR) e1a2 fusion transcript/control transcript
propertyNRto  =  Number Ratio
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
scaleQn  =  Quantitative:  The result of the test is a numeric value that relates to a continuous numeric scale. Reported either as an integer, a ratio, a real number, or a range. The test result value may optionally contain a relational operator from the set {<=, <, >, >=}. Valid values for a quantitative test are of the form "7", "-7", "7.4", "-7.4", "7.8912", "0.125", "<10", "<10.15", ">12000", 1-10, 1:256
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)e1a2/control Bld/T

Basic Attributes

classMOLPATH.TRNLOC
type1  Laboratory
order vs. observationObservation
example UCUM units%
The Unified Code for Units of Measure (UCUM) is a code system intended to include all units of measures being contemporarily used in international science, engineering, and business (www.unitsofmeasure.org)
example unit%

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.

Member of these Panels

72104-3Acute and chronic leukemia fusion transcript per control transcript panel - Blood or Tissue by Molecular genetics method
52135-1t(9;22)(q34.1;q11)(ABL1,BCR) transcript detection panel - Blood or Tissue by Molecular genetics method

History/Usage

test rank4256 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 reasonWe changed the property from NFr to NRto. We had misunderstood how this test was done - it counts the number of transcripts of the two transcripts produced (usually) by PCR. Updated Component part to harmonize with ISCN guidelines and current LOINC nomenclature.

Related Names

ABL
ABL1
ABL1 transcript
ALL
bcr/abl
BCR1
bcr-abl1
Blood
Breakpoint cluster region
Chronic myeloid leukemia
CML
control gene
D22S11
D22S662
DNA
gene fusion
gene translocation
Genetics
Heredity
Heritable
Inherited
JTK7
major breakpoints
Mbr
Mcr
minor breakpoints
Molecular genetics
Molecular pathology
MOLPATH
MOLPATH.TRANSLOCATION
Number ratio
p150
PCR
Ph chromosome
Philadelphia chromosome
PHL
Point in time
QNT
Quan
Quant
Quantitative
Random
RNA
T prime
t(9,22)(ABL1,BCR) gene translocation
t(9,22)(ABL1,BCR) p190 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)e1a2
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.

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