79211-9
LaboratoryFetal Chromosome X and Y aneuploidy risk [interpretation] in Plasma cell-free DNA Qualitative by Sequencing
Definition
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.
LOINC 6-Axis Classification
Component
Fetal chromosome X & Y aneuploidy risk
Property
Imp
Time Aspect
Pt
System
Plas.cfDNA
Scale Type
Ord
Method Type
Sequencing
Details
Class
MOLPATH
Order/Observation
Observation
Short Name
Fet X + Y aneup risk Plas.cfDNA Seq-Imp
Display Name
Chr X and Y aneuploidy risk Sequencing Ql (cfDNA) [Interp]
Related Names
Frequently Asked Questions
What is LOINC code 79211-9?
LOINC code 79211-9 identifies "Fetal Chromosome X and Y aneuploidy risk [interpretation] in Plasma cell-free DNA Qualitative by Sequencing". 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.
What does 79211-9 measure?
This code measures Fetal chromosome X & Y aneuploidy risk in Plas.cfDNA. It belongs to the MOLPATH class in the LOINC classification.
What is LOINC?
LOINC (Logical Observation Identifiers Names and Codes) is a universal standard for identifying laboratory and clinical observations. It is maintained by the Regenstrief Institute and used worldwide for health data exchange.