Chromosome rearrangement [Identifier] in Blood or Tissue by Mate pair sequencing Nominal   94592-3

LOINC Code


LOINC code94592-3
nameChromosome rearrangement [Identifier] in Blood or Tissue by Mate pair sequencing Nominal
descriptionThis term is used to report the mate pair sequencing results, preferably using a standardize nomenclature such as ISCN, for targeted chromosome analysis of neoplastic clones in blood or bone marrow specimens. Testing is performed in patients with acute myeloid leukemia (AML) or other myeloid malignancies when previous cytogenetic studies are unsuccessful or detect a chromosome abnormality of unknown significance. Results provide diagnostic, prognostic, and therapeutic information for patient care.
statusACTIVE

Fully-Specified Name

componentChromosome rearrangement
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.
methodMate pair sequencing

Additional Names

short nameAML chromo analys Bld/Mar MPSeq

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 updated2.68
last change typeADD  - added

Related Names

Blood
Chromosom
Chromosomes
Genetics
Heredity
Heritable
high-throughput sequencing
HTS
Identity or presence
Inherited
Molecular pathology
MOLPATH
MPSeq
Next generation sequencing
NGS
Nominal
Point in time
Random
Tissue
Tissue, unspecified
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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