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{component}   LP432695-7

Laboratory   LP29693-6

Lab terms not yet categorized   LP248770-2

t(8;21)(q22;q22.3)(RUNX1T1,RUNX1) fusion transcript [Presence] in Blood or Tissue by Molecular genetics method   21819-8

LOINC Code


LOINC code21819-8
namet(8;21)(q22;q22.3)(RUNX1T1,RUNX1) fusion transcript [Presence] in Blood or Tissue by Molecular genetics method
statusACTIVE

Fully-Specified Name

componentt(8;21)(q22;q22.3)(RUNX1T1,RUNX1) fusion transcript
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(8;21)(RUNX1T1,RUNX1) 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.

Member of these Panels

72103-5Acute and chronic leukemia fusion transcript panel - Blood or Tissue by Molecular genetics method

History/Usage

test rank5876 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 reasonChanged gene names CBFA2T1 to RUNX1T1 and CBFA2 to RUNX1, the recommended gene names by the HUGO Gene Nomenclature Committee (HGNC). Updated Component part to harmonize with ISCN guidelines and current LOINC nomenclature.

Related Names

21q22.3
Acute myelogenous leukemia 1 translocation 1, cyclin-D related
Acute myeloid leukemia
Acute myeloid leukemia 1
AML
AML1
AML1T1L myeloid translocation gene on 8q22
Arbitrary
Blood
CBFA2
CBFA2T1
CDR
Core binding factor runt domain alpha subunit 2
DNA
ETO
gene fusion
gene translocation
Genetics
Heredity
Heritable
Inherited
MGC2796
Molecular genetics
Molecular pathology
 MOLPATH
MOLPATH.TRANSLOCATION
MTG8
Ordinal
PCR
Point in time
QL
Qual
Qualitative
Random
RNA
Screen
T prime
t(8,21)(RUNX1T1,RUNX1) gene translocation
t(8
21)(RUNX1T1,RUNX1)
Tissue
Tissue, unspecified
translocation
WB
Whole blood
Whole blood or Tissue
ZMYND2

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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