Chromosome region 11p15 methylation and deletion+duplication in Amniotic fluid by Molecular genetics method   81850-0

LOINC Code


LOINC code81850-0
nameChromosome region 11p15 methylation and deletion+duplication in Amniotic fluid by Molecular genetics method
descriptionThe methylation status and copy numbers of the 11p15 chromosome region can be determined by various methods, including methylation-specific PCR and multiplex ligation-dependent probe amplification (MS-MLPA). This test is performed to detect causes of Beckwith-Wiedemann Syndrome (BWS) and Russell-Silver Syndrome (RSS).
statusACTIVE

Fully-Specified Name

componentChromosome region 11p15 methylation & deletion+duplication
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 nameChr 11p15 Methyl + Del+Dup Amn

Basic Attributes

classMOLPATH
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
Amn
Amn fl
Amnio
Amniotic flu
Amniotic fluid
Amplification
Beckwith Wiedemann Syndrome
BWS
Chr 11p15
Chr 11p15 methylation + deletion+duplication
Chromosom
Chromosomes
Cyto loc
Del
Del+Dup
Deletions
Document
Dp
Finding
Findings
Genetics
Gyn
Gynecology
Heredity
Heritable
Inherited
Methyl + Del+Dup
Molecular genetics
Molecular pathology
MOLPATH
OB
ObGyn
Obstetrics
PCR
Point in time
Random
RSS
Russell-Silver Syndrome

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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