Complex variant name Nominal 81261-0
LOINC Code
LOINC code | 81261-0 | ||
---|---|---|---|
name | Complex variant name Nominal | ||
description | This 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/] | ||
status | TRIAL | ||
Fully-Specified Name | |||
component | Complex variant name | ||
property | Find = Finding | ||
time | Pt = 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 | ||
scale | Nom = 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 name | Comp var name | ||
Basic Attributes | |||
class | MOLPATH | ||
type | 1 Laboratory | ||
order vs. observation | Observation | ||
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 updated | 2.58 | ||
last change type | MIN - change to field other than name | ||
Related Names | |||
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