CDKN2A gene deletion+duplication and full mutation analysis in Blood or Tissue by Molecular genetics method   89037-6

LOINC Code


LOINC code89037-6
nameCDKN2A gene deletion+duplication and full mutation analysis in Blood or Tissue by Molecular genetics method
statusACTIVE

Fully-Specified Name

componentCDKN2A gene deletion+duplication & full mutation analysis
propertyFind  =  Finding
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
scaleDoc  =  Document:  A document that could be in many formats (XML, narrative, etc.)
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 nameCDKN2A Del+Dup + Full Mut Anl Bld/T

Basic Attributes

classMOLPATH
type1  Laboratory
order vs. observationBoth

Ask At Order Entry

Ask at Order Entry (AOE) observations for a clinical observation or laboratory test. A LOINC term may represent a single AOE observation or a panel containing several AOE observations.

81247-9Master HL7 genetic variant reporting panel

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 updated2.65
last change typeMIN  - change to field other than name

Related Names

Amplification
ARF
Blood
CDK4 inhibitor
CDK4I
CDKN2
CMM2
Cyclin-dependent kinase 4 inhibitor A gene
cyclin-dependent kinase inhibitor 2A
Cyclin-dependent kinase inhibitor 2A gene
Del
Del+Dup
Del+Dup + Full Mut Anl
Deletions
Document
Dp
Finding
Findings
full gene sequencing
Full Mut Anl
Genetics
Heredity
Heritable
Inherited
INK4
INK4a
Melanoma
MLM
Molecular genetics
Molecular pathology
MOLPATH
MTS1
MTS-1
Multiple tumor suppressor 1
Mut
Mutations
P14
P14ARF
p16
P16INK4
P16INK4A
P16-INK4A
P19
P19ARF
PCR
Point in time
Random
sequencing of entire coding region
Tissue
Tissue, unspecified
TP16
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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