Fetal Chromosome X and Y aneuploidy risk [interpretation] in Plasma cell-free DNA Qualitative by Sequencing 79211-9
LOINC Code
| LOINC code | 79211-9 | ||
|---|---|---|---|
| name | Fetal Chromosome X and Y aneuploidy risk [interpretation] in Plasma cell-free DNA Qualitative by Sequencing | ||
| description | The risk interpretation (e.g. increased risk) of chromosome X & Y aneuploidy 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 chromosome X & Y aneuploidy. | ||
| status | ACTIVE | ||
Fully-Specified Name | |||
| component | Fetal chromosome X & Y aneuploidy 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 X + Y aneup 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. | |||
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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