LOINC Home

{component}   LP432695-7

Laboratory   LP29693-6

Lab terms not yet categorized   LP248770-2

F8 gene intron 1 and 22 inversion targeted mutation analysis in Amniotic fluid or Chorionic villus sample by Molecular genetics method   82343-5

LOINC Code


LOINC code82343-5
nameF8 gene intron 1 and 22 inversion targeted mutation analysis in Amniotic fluid or Chorionic villus sample by Molecular genetics method
statusACTIVE

Fully-Specified Name

componentF8 gene intron 1 & 22 inversion 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 nameF8 intron 1+22 Inv Mut Anl Amn/CVS

Basic Attributes

classMOLPATH.INV
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

AF
AHF
Amn
Amn fl
Amn/CVS
Amnio
Amniotic flu
Amniotic fluid
Chorionic villi
Chorionic villus sample
Classic hemophilia
Coagulation Factor VIII gene
coagulation factor VIII, procoagulant component
Document
DXS1253E
F8 intron 1+22 Inv
F8B
F8C
Factor 8
Finding
Findings
FVIII
FVIII gene
Genetics
 Gyn
Gynecology
Haemophilia
HEMA
Hemophilia A
Heredity
Heritable
i
Inherited
Molecular genetics
Molecular pathology
MOLPATH
MOLPATH.INV
Mut
Mut Anl
Mutations
OB
ObGyn
Obstetrics
PCR
Point in time
Procoagulant component
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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