HTT gene CAG repeats [Presence] in Blood or Tissue by Molecular genetics method   21763-8

LOINC Code


LOINC code21763-8
nameHTT gene CAG repeats [Presence] in Blood or Tissue by Molecular genetics method
descriptionCopy number >36 is considered abnormal and an indication of Huntington disease (HD).
statusACTIVE

Fully-Specified Name

componentHTT gene.CAG repeats
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 nameHTT gene CAG Rpt Bld/T Ql

Basic Attributes

classMOLPATH.NUCREPEAT
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.

Member of these Panels

53783-7HTT gene mutation panel - Blood or Tissue by Molecular genetics method

History/Usage

test rank11842 of 2000 most commonly performed tests by labs in USA
first released
last updated2.73
last change typeMIN  - change to field other than name
change reasonChanged gene name from HD to HTT, the current (2012) approved HUGO gene name. June 2015: Changed Property from Arb (Arbitrary) to 'Threshold' since the results (e.g. positive, intermediate, negative) is based on the number of nucleotide repeats. Moved term from Class MOLPATH.TRINUC to MOLPATH.NUCREPEAT, a Class used to group together observations for nucleotide repeats.; 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

5HTT
5-HTT
5-HTTLPR
Blood
Genetics
HD gene
Heredity
Heritable
hSERT
HTT
HTT gene CAG Rpt
huntingtin
Huntington chorea
Huntington disease
Huntington's disease
Inherited
IT15
Molecular genetics
Molecular pathology
MOLPATH
MOLPATH.NUCREPEAT
Neuro
Neurology
OCD1
Ordinal
PCR
Point in time
PR
QL
Qual
Qualitative
Random
Repeat
Screen
SERT
SERT1
solute carrier family 6 (neurotransmitter transporter), member 4
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.

demo
request yours today
subscribe
start today
newsletter
free subscription

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