t(9;22)(q34.1;q11)(ABL1,BCR) fusion transcript major break points [Presence] in Blood or Tissue by Molecular genetics method   21822-2

LOINC Code


LOINC code21822-2
namet(9;22)(q34.1;q11)(ABL1,BCR) fusion transcript major break points [Presence] in Blood or Tissue by Molecular genetics method
statusACTIVE

Fully-Specified Name

componentt(9;22)(q34.1;q11)(ABL1,BCR) fusion transcript major break points
propertyArb  =  Arbitrary
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(9;22)(ABL1,BCR) Major Bld/T Ql

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 rank8094 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 reasonUpdated Component part to harmonize with ISCN guidelines and current LOINC nomenclature.; Changed Order_Obs from 'Observation Only' to 'Both' to fit current order use cases.

Related Names

ABL
ALL
Arbitrary
b2a2
b2a2+b3a2
b2a3
b3a2
b3a3
bcr/abl
BCR1
bcr-abl1
Blood
breakpoint
Breakpoint cluster region
c3a2
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
MOLPATH.TRANSLOCATION
Ordinal
p150
p210
PCR
Ph chromosome
Philadelphia chromosome
PHL
Point in time
QL
Qual
Qualitative
Random
RNA
Screen
T prime
t(9,22)(ABL1,BCR) gene translocation
t(9,22)(ABL1,BCR) gene translocation major break points
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.

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