SEPT9 gene targeted mutation analysis in Blood or Tissue by Molecular genetics method   77067-7

LOINC Code


LOINC code77067-7
nameSEPT9 gene targeted mutation analysis in Blood or Tissue by Molecular genetics method
statusACTIVE

Fully-Specified Name

componentSEPT9 gene targeted 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 nameSEPT9 gene Mut Anl Bld/T

Basic Attributes

classMOLPATH.MUT
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.

77313-5DNA analysis discrete sequence variation basic associated observations panel - Blood or Tissue by Molecular genetics method

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
change reasonBased 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

Acute myelomonocytic leukemia
AF17q25
Blood
Document
Finding
Findings
Genetics
Hereditary neuralgic amyotrophy
Heredity
Heritable
HNA
Inherited
MLL septin-like fusion
Molecular genetics
Molecular pathology
MOLPATH
MOLPATH.MUTATIONS
MSF
MSF1
Mut
Mut Anl
Mutations
NAPB
PCR
PNUTL4
Point in time
Random
SeptD1
septin 9
SINT1
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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