Fetal Microdeletions risk [interpretation] in Plasma cell-free DNA Qualitative by Sequencing 79212-7
LOINC Code
LOINC code | 79212-7 | ||
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name | Fetal Microdeletions risk [interpretation] in Plasma cell-free DNA Qualitative by Sequencing | ||
description | The interpretation (e.g. not detected, increased risk) of chromosomal microdeletions present in fetal cell-free DNA from maternal plasma. This term was created for, but not limited in use to, QNatal Advanced, a non-invasive prenatal test which uses massively parallel sequencing to identify microdeletions in select chromosome regions, including 22q (DiGeorge syndrome), 15q (Prader-Willi/Angelman syndromes), 11q (Jacobsen syndrome), 8q (Langer-Giedion syndrome), 5p (Cri-du-chat syndrome), 4p (Wolf-Hirschhorn syndrome), and 1p36 deletion syndrome. | ||
status | ACTIVE | ||
Fully-Specified Name | |||
component | Fetal microdeletions risk | ||
property | Imp = Impression/interpretation of study | ||
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 | Ord = Ordinal: Ordered categorical responses, e.g., 1+, 2+, 3+; positive, negative; reactive, indeterminate, nonreactive. | ||
method | Sequencing | ||
Additional Names | |||
short name | Fet Microdel risk Plas.cfDNA Seq-Imp | ||
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. | |||
Member of these Panels | |||
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History/Usage | |||
first released | |||
last updated | 2.66 | ||
last change type | NAM - change to Analyte/Component | ||
change reason | Added "Fetal" to Component to clarify that the result is about the fetus. | ||
Related Names | |||
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