Complex variant name Nominal   81261-0

LOINC Code


LOINC code81261-0
nameComplex variant name Nominal
descriptionThis term is used to report the formal name of a complex variant, including the reference sequence and details about the variation. For example, NM_000106.5(CYP2D6):c.[886C>T;457G>C] - Haplotype represents a CYP2D6 gene variant with haplotype nucleotide changes c.886C>T and c.457G>C and the NCBI reference sequence NM_000106.5. [http://www.ncbi.nlm.nih.gov/clinvar/variation/16895/]
statusTRIAL

Fully-Specified Name

componentComplex variant name
propertyFind  =  Finding
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.
system^Patient
scaleNom  =  Nominal:  Nominal or categorical responses that do not have a natural ordering. (e.g., names of bacteria, reported as answers, categories of appearance that do not have a natural ordering, such as, yellow, clear, bloody.
method

Additional Names

short nameComp var name

Basic Attributes

classMOLPATH
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 updated2.58
last change typeMIN  - change to field other than name

Related Names

Comp var
Comp var name
Compx
Finding
Findings
Molecular pathology
MOLPATH
Nominal
Point in time
Random

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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