FGFR3 gene p.Gly380Arg targeted mutation analysis in Amniotic fluid or Chorionic villus sample by Molecular genetics method   82137-1

LOINC Code


LOINC code82137-1
nameFGFR3 gene p.Gly380Arg targeted mutation analysis in Amniotic fluid or Chorionic villus sample by Molecular genetics method
statusACTIVE

Fully-Specified Name

componentFGFR3 gene.p.Gly380Arg 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/CVS
    Amnio 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 nameFGFR3 p.G380R Mut Anl Amn/CVS

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.

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

ACH
Achondroplasia
AF
Amn
Amn fl
Amn/CVS
Amnio
Amniotic flu
Amniotic fluid
CD333
CEK2
Chorionic villi
Chorionic villus sample
Document
FGFR3 Gly380Arg
FGFR3 p.G380R
fibroblast growth factor receptor 3
Finding
Findings
Genetics
Gyn
Gynecology
Heredity
Heritable
HSFGFR3EX
Inherited
JTK4
Molecular genetics
Molecular pathology
MOLPATH
MOLPATH.MUTATIONS
Mut
Mut Anl
Mutations
OB
ObGyn
Obstetrics
P prime
PCR
Point in time
Random
Thanatophoric dwarfism
Thanatophoric dysplasia

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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