AutoICD API

75584-3

Laboratory

Fetal Prader-Willi syndrome risk [Interpretation] based on Plasma cell-free+WBC DNA by Dosage of chromosome-specific cfDNA Qualitative

Definition

This term was developed for, but is not limited in use to, Natera's Panorama noninvasive prenatal test for fetal aneuploidies and microdeletions.

LOINC 6-Axis Classification

Component

Fetal Prader-Willi syndrome risk

Property

Imp

Time Aspect

Pt

System

WBC.DNA+Plas.cfDNA

Scale Type

Ord

Method Type

Dosage of chromosome specific cf DNA

Details

Class

MOLPATH.DEL

Order/Observation

Both

Short Name

Fet PWS risk WBC.DNA+cfDNA Ql

Display Name

Prader-Willi syndrome risk Dosage of chromosome-specific cfDNA Ql (Plasma cell-free+WBC DNA) [Interp]

Related Names

ChromosomChromosomesGeneticsHeredityHeritableImpressionImpression/interpretation of studyImpressionsInheritedInterpInterpretationLeukocytesMolecular pathologyMOLPATHMOLPATH.DELETIONSOrdinalPlPlasmaPlsmPoint in timePWS riskQlQualQualitativeRandomScreenSpecWBC.DNA+cfDNAWBCsWhite blood cells

Frequently Asked Questions

What is LOINC code 75584-3?

LOINC code 75584-3 identifies "Fetal Prader-Willi syndrome risk [Interpretation] based on Plasma cell-free+WBC DNA by Dosage of chromosome-specific cfDNA Qualitative". This term was developed for, but is not limited in use to, Natera's Panorama noninvasive prenatal test for fetal aneuploidies and microdeletions.

What does 75584-3 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.