AutoICD API

75557-9

Laboratory

Fetal Trisomy 18 risk [Likelihood] based on Plasma cell-free+WBC DNA by Dosage of chromosome-specific cfDNA Narrative

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 trisomy 18 risk

Property

Likelihood

Time Aspect

Pt

System

WBC.DNA+Plas.cfDNA

Scale Type

Nar

Method Type

Dosage of chromosome specific cf DNA

Details

Class

MOLPATH.TRISOMY

Order/Observation

Both

Short Name

Fet Ts 18 risk WBC.DNA+cfDNA

Display Name

Trisomy 18 risk Dosage of chromosome-specific cfDNA Nar (Plasma cell-free+WBC DNA)

Related Names

ChromosomChromosomesEdward syndromeGeneticsHeredityHeritableInheritedLeukocytesMolecular pathologyMOLPATHMOLPATH.TRISOMYNarrativePlPlasmaPlsmPoint in timeRandomReportRiskSpecT18 riskTsTs 18 riskWBC.DNA+cfDNAWBCsWhite blood cells

Frequently Asked Questions

What is LOINC code 75557-9?

LOINC code 75557-9 identifies "Fetal Trisomy 18 risk [Likelihood] based on Plasma cell-free+WBC DNA by Dosage of chromosome-specific cfDNA Narrative". 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 75557-9 measure?

This code measures Fetal trisomy 18 risk in WBC.DNA+Plas.cfDNA. It belongs to the MOLPATH.TRISOMY 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.