NF2 gene mutations found [Identifier] in Amniotic fluid by Molecular genetics method Nominal   45332-4

LOINC Code


LOINC code45332-4
nameNF2 gene mutations found [Identifier] in Amniotic fluid by Molecular genetics method Nominal
statusACTIVE

Fully-Specified Name

componentNF2 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.
systemAmnio fld  =  Amniotic fluid
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 nameNF2 gene Mut Anl Amn

Basic Attributes

classMOLPATH.MUT
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

54043-5HEDIS 2009 Codes to identify sexually active women (CHL-B)
57818-7HEDIS 2010 Codes to identify sexually active women (CHL-B)
60444-7HEDIS 2011 Codes to identify sexually active women (CHL-B)
67766-6HEDIS 2012 Codes to identify sexually active women (CHL-B)
72198-5HEDIS 2013 Codes to identify sexually active women (CHL-B)
74258-5HEDIS 2014 Value Set - Sexual Activity

History/Usage

first released
last updated2.63
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

ACN
AF
Amn
Amn fl
Amnio
Amniotic flu
Amniotic fluid
BANF
Genetics
Gyn
Gynecology
Heredity
Heritable
Identity or presence
Inherited
Merlin
Molecular genetics
Molecular pathology
MOLPATH
MOLPATH.MUTATIONS
Mut
Mut Anl
Mutations
Neurofibromin 2
neurofibromin 2 (merlin)
Nominal
OB
ObGyn
Obstetrics
PCR
Point in time
Random
SCH
Schwannomerlin
Schwannomin

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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