Noninvasive prenatal fetal 18 and 21 aneuploidy panel - Plasma cell-free DNA by Sequencing 77019-8
LOINC Code
LOINC code | 77019-8 | ||
---|---|---|---|
name | Noninvasive prenatal fetal 18 and 21 aneuploidy panel - Plasma cell-free DNA by Sequencing | ||
description | This term was created for, but is not limited in use to, Sequenom Laboratories' VisibiliT panel, which analyzes circulating cell-free DNA extracted from maternal plasma using whole genome sequencing to determine the risk for fetal chromosome 18 and 21 aneuploidies. VisibiliT is indicated for use in pregnant women with average risk for fetal chromosomal aneuploidy. | ||
status | ACTIVE | ||
Fully-Specified Name | |||
component | Noninvasive prenatal fetal 18 & 21 aneuploidy panel | ||
property | - | ||
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 | Plas.cfDNA | ||
scale | - | ||
method | Sequencing | ||
Additional Names | |||
short name | NIP fet 18+21 aneu pnl Plas.cfDNA Seq | ||
Basic Attributes | |||
class | PANEL.MOLPATH | ||
type | 1 Laboratory | ||
order vs. observation | Order | ||
Panel Components | |||
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 | 2.73 | ||
last change type | MIN - change to field other than name | ||
Related Names | |||
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