UGT2B15 gene mutations found [Identifier] in Blood or Tissue by Molecular genetics method Nominal   72881-6

LOINC Code


LOINC code72881-6
nameUGT2B15 gene mutations found [Identifier] in Blood or Tissue by Molecular genetics method Nominal
descriptionA patient's genotype for the UGT2B15 gene is typically reported as *A/*B where A is the allele from one chromosome and B is the allele from the other chromosome. The genotype is determined by the analysis of specific single nucleotide polymorphisms (SNPs) within the gene by various molecular techniques, including PCR and microarray. In some cases, SNP results are analyzed by bioinformatics computer software to determine a patient's overall genotype.
statusACTIVE

Fully-Specified Name

componentUGT2B15 gene targeted mutation analysis
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 nameUGT2B15 Mut Anl Bld/T

Basic Attributes

classMOLPATH.PHARMG
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 updated2.67
last change typeMAJ  - change to name field other than Component;
change reasonRelease 2.67: CLASS: Updated to MOLPATH.PHARMG, the more representative LOINC Class for this concept.; SYSTEM: Updated System from "Bld/Tiss/Sal" to "Bld/Tiss" since this System in LOINC encompasses all specimens used for germline nucleic acid testing, including blood, tissue and cells contained in swabs as well as fluids such as saliva.; Previous Releases: Based on LOINC Committee review (June 2016), "targeted" was added to the Component to clarify that this test is looking for a specific set of mutations as described in the LOINC User Guide under the Molecular Genetics section.

Related Names

Blood
Genetics
Heredity
Heritable
HLUG4
Identity or presence
Inherited
Molecular genetics
Molecular pathology
MOLPATH
MOLPATH.PHARMG
Mut
Mut Anl
Mutations
Nominal
PCR
Point in time
Random
Tissue
Tissue, unspecified
UDP glucuronosyltransferase 2 family, polypeptide B15
UDPGT 2B8
UDPGT2B15
UDPGTH3
UGT2B8
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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