FMR1 gene targeted mutation analysis in Amniotic fluid by Molecular genetics method   45327-4

LOINC Code


LOINC code45327-4
nameFMR1 gene targeted mutation analysis in Amniotic fluid by Molecular genetics method
statusACTIVE

Fully-Specified Name

componentFMR1 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.
systemAmnio fld  =  Amniotic fluid
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 nameFMR1 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

test rank11254 of 2000 most commonly performed tests by labs in USA
first released
last updated2.73
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.; Based on LOINC Committee review (June 2019), updated the Property from "Prid" to "Find" and Scale from "Nar" to "Doc" to align with the current LOINC model for naming collections of information reported in narrative and/or structured formats.

Related Names

AF
Amn
Amn fl
Amnio
Amniotic flu
Amniotic fluid
Document
Finding
Findings
FMRP
Fragile X
Fragile X mental retardation 1
Fragile X syndrome
FRAXA
Genetics
Gyn
Gynecology
Heredity
Heritable
Inherited
Molecular genetics
Molecular pathology
MOLPATH
MOLPATH.MUTATIONS
Mut
Mut Anl
Mutations
OB
ObGyn
Obstetrics
PCR
POF
POF1
Point in time
Random

Copyright © 2023 Regenstrief Institute, Inc. All Rights Reserved. To the extent included herein, the LOINC table and LOINC codes are copyright © 1995-2023, 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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