79211-9
LOINC Code
| LOINC code | 79211-9 | |
|---|---|---|
| name | ||
| 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 | Chr X + Y aneup; Chr X + Y aneup risk; Chromosom; Chromosomes; Genetics; Heredity; Heritable; high-throughput sequencing; HTS; Impression; Impression/interpretation of study; Impressions; Inherited; Interp; Interpretation; Molecular pathology; MOLPATH; Ne | |
Basic Attributes | ||
| class | MOLPATH | |
| type | 1 Laboratory | |
| order vs. observation | Fet X + Y aneup | |
History/Usage | ||
| first released | ||
| last updated | 2.66 | |
| last change type | NAM - change to Analyte/Component | |
Related Names | ||
Copyright © 2026 Regenstrief Institute, Inc. All Rights Reserved. To the extent included herein, the LOINC table and LOINC codes are copyright © 1995-2026, 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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