21763-8

LOINC Code


LOINC code21763-8
name
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 name5HTT; 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.NUCREPE

Basic Attributes

classMOLPATH.NUCREPEAT
type1  Laboratory
order vs. observationHTT gene CAG Rp

Member of these Panels

53783-7

History/Usage

first released
last updated2.73
last change typeMIN  - change to field other than name

Related Names



Copyright © 2026 Regenstrief Institute, Inc. All Rights Reserved. To the extent included herein, the LOINC table and LOINC codes are copyright © 1995-2026, 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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