AutoICD API

75577-7

Laboratory

Fetal 22q11.2 deletion 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 22q11.2 deletion 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.DEL

Order/Observation

Both

Short Name

Fet 22q11.2 del risk WBC.DNA+cfDNA

Display Name

22q11.2 del risk Dosage of chromosome-specific cfDNA Nar (Plasma cell-free+WBC DNA)

Related Names

22q11.2 del riskChromosomChromosomesLeukocytesMolecular pathologyMOLPATHMOLPATH.DELETIONSNarrativePlPlasmaPlsmPoint in timeRandomReportRiskSpecWBC.DNA+cfDNAWBCsWhite blood cells

Frequently Asked Questions

What is LOINC code 75577-7?

LOINC code 75577-7 identifies "Fetal 22q11.2 deletion 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 75577-7 measure?

This code measures Fetal 22q11.2 deletion 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.