PMP22 gene allele 1 [Presence] in Blood or Tissue by Molecular genetics method   35324-3

LOINC Code


LOINC code35324-3
namePMP22 gene allele 1 [Presence] in Blood or Tissue by Molecular genetics method
statusACTIVE

Fully-Specified Name

componentPMP22 gene allele 1
propertyPrThr  =  Present or threshold:  The Property PrThr stands for “Presence or Threshold”, meaning either a) the actual presence or absence of an analyte, or b) that the amount of analyte detected is over some predetermined threshold.
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
scaleOrd  =  Ordinal:  Ordered categorical responses, e.g., 1+, 2+, 3+; positive, negative; reactive, indeterminate, nonreactive.
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 namePMP22 allele1 Bld/T Ql

Basic Attributes

classMOLPATH.MUT
type1  Laboratory
order vs. observationObservation

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 updated2.56
last change typeMIN  - change to field other than name
change reasonThe PrThr property is used for LOINC terms whose results are reported using an ordered categorical scale, regardless of whether or not an internal threshold was used to make that determination. This change was approved by the Laboratory LOINC Committee in June 2016.

Related Names

Blood
Charcot-Marie Tooth disease
CMT
CMT1A
CMT1E
Dejerine-Sottas syndrome
DSS
GAS3
GAS-3
Genetics
Growth arrest specific gene 3
Hereditary neuropathy with liability to pressure palsies
Heredity
Heritable
HMSNIA
HNPP
i
Inherited
Molecular genetics
Molecular pathology
MOLPATH
MOLPATH.MUTATIONS
Ordinal
PCR
Peripheral myelin protein 22
PMP-22
PMP22 allele1
Point in time
PR
QL
Qual
Qualitative
Random
Screen
Sp110
Tissue
Tissue, unspecified
WB
Whole blood
Whole blood or Tissue

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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