PEX2 gene targeted mutation analysis in Blood or Tissue by Molecular genetics method   101960-3

LOINC Code


LOINC code101960-3
namePEX2 gene targeted mutation analysis in Blood or Tissue by Molecular genetics method
statusACTIVE

Fully-Specified Name

componentPEX2 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.
systemBld/Tiss
    Bld  =  Whole blood
    Tiss  =  Tissue, unspecified
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 namePEX2 gene Mut Anl Bld/T

Basic Attributes

classMOLPATH.MUT
type1  Laboratory
order vs. observationBoth
formula (readable)N/A

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 updated2.75
last change typeADD  - added

Related Names

Blood
Document
Finding
Findings
Molecular genetics
Molecular pathology
MOLPATH
MOLPATH.MUTATIONS
Mut
Mut Anl
Mutations
PCR
peroxin 2
peroxisomal biogenesis factor 2
peroxisomal membrane protein 3 (35kD, Zellweger syndrome)
peroxisomal membrane protein 3, 35kDa
PEX2 Mut Anl
Point in time
Random
Tissue
Tissue, unspecified
WB
Whole blood
Whole blood or Tissue
Zellweger syndrome

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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