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{component}   LP432695-7

Laboratory   LP29693-6

Lab terms not yet categorized   LP248770-2

Chromosome region Xp22.33 AndOr Yp11.32 deletion and duplication mutation analysis in Blood or Tissue by MLPA   81873-2

LOINC Code


LOINC code81873-2
nameChromosome region Xp22.33 AndOr Yp11.32 deletion and duplication mutation analysis in Blood or Tissue by MLPA
descriptionDetection of deletions or duplications in the Xp22.33 and Yp11.32 regions of the sex chromosomes, which contain the pseudoautosomal region 1 (PAR1) and SHOX gene, by MLPA analysis. This term was created for, but not limited in use to, the submitter's kit, SALSA MLPA P018 SHOX probemix.
statusACTIVE

Fully-Specified Name

componentChromosome region Xp22.33 &or Yp11.32 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.
systemBld/Tiss
    Bld  =  Whole blood
    Tiss  =  Tissue, unspecified
scaleDoc  =  Document:  A document that could be in many formats (XML, narrative, etc.)
methodMLPA

Additional Names

short nameXp22.33 +or Yp11.32 Del+Dup Bld/T MLPA

Basic Attributes

classMOLPATH.DELDUP
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

Amplification
Blood
Chr Xp22.33 +or Yp11.32 deletion+duplication
Chromosom
Chromosomes
Cyto loc
Del
Del+Dup
Deletions
Document
Dp
Finding
Findings
Genetics
Heredity
 Heritable
Inherited
Molecular pathology
MOLPATH
MOLPATH.DELDUP
Point in time
Random
SHOX
Tissue
Tissue, unspecified
WB
Whole blood
Whole blood or Tissue
Xp22.33 +or Yp11.32

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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