75582-7
LaboratoryFetal Prader-Willi syndrome risk [Likelihood] based on Plasma cell-free+WBC DNA by Dosage of chromosome-specific cfDNA
Definition
This term was developed for, but is not limited in use to, Natera's Panorama noninvasive prenatal test for fetal aneuploidies and microdeletions. It represents the risk based on a priori risk combined with the Panorama test result.
LOINC 6-Axis Classification
Component
Fetal Prader-Willi syndrome risk
Property
Likelihood
Time Aspect
Pt
System
WBC.DNA+Plas.cfDNA
Scale Type
Qn
Method Type
Dosage of chromosome specific cf DNA
Details
Class
MOLPATH.DEL
Order/Observation
Both
Short Name
Fet PWS risk WBC.DNA+cfDNA Qn
Display Name
Prader-Willi syndrome risk Dosage of chromosome-specific cfDNA Qn (Plasma cell-free+WBC DNA)
Related Names
Frequently Asked Questions
What is LOINC code 75582-7?
LOINC code 75582-7 identifies "Fetal Prader-Willi syndrome risk [Likelihood] based on Plasma cell-free+WBC DNA by Dosage of chromosome-specific cfDNA". This term was developed for, but is not limited in use to, Natera's Panorama noninvasive prenatal test for fetal aneuploidies and microdeletions. It represents the risk based on a priori risk combined with the Panorama test result.
What does 75582-7 measure?
This code measures Fetal Prader-Willi syndrome risk in WBC.DNA+Plas.cfDNA. It belongs to the MOLPATH.DEL 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.