t(9;22)(q34.1;q11)(ABL1,BCR) fusion transcript break points [Identifier] in Blood or Tissue by Molecular genetics method Nominal   75892-0

LOINC Code


LOINC code75892-0
namet(9;22)(q34.1;q11)(ABL1,BCR) fusion transcript break points [Identifier] in Blood or Tissue by Molecular genetics method Nominal
descriptionUsed to report the major (p210), minor (p190), and micro (p230) BCR-ABL1 breakpoints, which together account for the vast majority of BCR-ABL1 gene fusion events in CML and ALL.
statusACTIVE

Fully-Specified Name

componentt(9;22)(q34.1;q11)(ABL1,BCR) fusion transcript break points
propertyPrid  =  Presence or identity:  Prid stands for “Presence or identity”, is used for assays that detect whether or not an analyte of a particular kind is present, and if it is, to identify the specific analyte.
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
scaleNom  =  Nominal:  Nominal or categorical responses that do not have a natural ordering. (e.g., names of bacteria, reported as answers, categories of appearance that do not have a natural ordering, such as, yellow, clear, bloody.
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) break pts 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

first released
last updated2.50
last change typeMIN  - change to field other than name

Related Names

ABL
ALL
bcr/abl
BCR1
bcr-abl1
Blood
break pts
breakpoint
Breakpoint cluster region
Chronic myeloid leukemia
CML
D22S11
D22S662
DNA
gene fusion
gene translocation
Genetics
Heredity
Heritable
Identity or presence
Inherited
JTK7
major breakpoints
Mbr
Mcr
minor breakpoints
Molecular genetics
Molecular pathology
MOLPATH
MOLPATH.TRANSLOCATION
Nominal
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 © 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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