88571-5
LaboratoryFetal Monosomy X risk [Interpretation] based on Plasma cell-free DNA by Dosage of chromosome-specific cfDNA Qualitative
Definition
The ordinal risk interpretation (e.g. high risk/low risk or high probability/low probability) of the fetus having monosomy X aneuploidy based on dosage of chromosome specific cell-free DNA (cf DNA) in maternal plasma that contains both fetal and maternal DNA. Results may also be based on the mother's current age, IVF status (self, non-self, or not applicable), and gestational age. This code is based, but not limited in use to, the submitter's test, the Harmony Prenatal Test, a non-invasive prenatal test for screening of fetal aneuploidy.
LOINC 6-Axis Classification
Component
Fetal monosomy X risk
Property
Imp
Time Aspect
Pt
System
Plas.cfDNA
Scale Type
Ord
Method Type
Dosage of chromosome specific cf DNA
Details
Class
MOLPATH
Order/Observation
Observation
Short Name
Fet Ms X risk Plas.cfDNA Ql
Display Name
Monosomy X risk Dosage of chromosome-specific cfDNA Ql (cfDNA) [Interp]
Related Names
Frequently Asked Questions
What is LOINC code 88571-5?
LOINC code 88571-5 identifies "Fetal Monosomy X risk [Interpretation] based on Plasma cell-free DNA by Dosage of chromosome-specific cfDNA Qualitative". The ordinal risk interpretation (e.g. high risk/low risk or high probability/low probability) of the fetus having monosomy X aneuploidy based on dosage of chromosome specific cell-free DNA (cf DNA) in maternal plasma that contains both fetal and maternal DNA. Results may also be based on the mother's current age, IVF status (self, non-self, or not applicable), and gestational age. This code is based, but not limited in use to, the submitter's test, the Harmony Prenatal Test, a non-invasive prenatal test for screening of fetal aneuploidy.
What does 88571-5 measure?
This code measures Fetal monosomy X 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.