HEXA gene p.Gly269Ser [Presence] in Blood or Tissue by Molecular genetics method   35382-1

LOINC Code


LOINC code35382-1
nameHEXA gene p.Gly269Ser [Presence] in Blood or Tissue by Molecular genetics method
statusACTIVE

Fully-Specified Name

componentHEXA gene.p.Gly269Ser
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 nameHEXA p.G269S Bld/T Ql

Basic Attributes

classMOLPATH.MUT
type1  Laboratory
order vs. observationBoth

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 reasonChanged Component part from g.G269S to p.G269S since variant is at described at protein level vs. genomic level. Changed Component name to align with the current HGVS recommendations to use the three letter codes for amnio acids. In the shortname, we kept the single letter codes.; The 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

beta-N-acetylhexosaminidase gene
Blood
Genetics
Gly269Ser
GM2-gangliosidosis
Heredity
Heritable
HEXA p.G269S
hexosaminidase A (alpha polypeptide)
hexosaminidase A (alpha polypeptide) gene
Inherited
Molecular genetics
Molecular pathology
MOLPATH
MOLPATH.MUTATIONS
N-acetyl-beta-glucosaminidase gene
Ordinal
P prime
PCR
Point in time
PR
QL
Qual
Qualitative
Random
rs121907954
Screen
Tay-Sachs disease
Tissue
Tissue, unspecified
TSD
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.

demo
request yours today
subscribe
start today
newsletter
free subscription

Thank you for choosing Find-A-Code, please Sign In to remove ads.