HEXA gene c.1277insTATC [Presence] in Blood or Tissue by Molecular genetics method   35472-0

LOINC Code


LOINC code35472-0
nameHEXA gene c.1277insTATC [Presence] in Blood or Tissue by Molecular genetics method
statusACTIVE

Fully-Specified Name

componentHEXA gene.c.1277insTATC
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 c.1277insTATC 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.1277 ins TATC to c.1277insTATC since variant is at coding level and to harmonize with HGVS nomenclature guidelines.; 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

1274_1277dupTATC
1277TATC
1278insTATC
beta-N-acetylhexosaminidase gene
Blood
Genetics
GM2-gangliosidosis
Heredity
Heritable
HEXA c.1277insTATC
hexosaminidase A (alpha polypeptide)
hexosaminidase A (alpha polypeptide) gene
Inherited
Molecular genetics
Molecular pathology
MOLPATH
MOLPATH.MUTATIONS
N-acetyl-beta-glucosaminidase gene
Ordinal
PCR
Point in time
PR
QL
Qual
Qualitative
Random
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.

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