Noninvasive prenatal fetal 18 & 21 aneuploidy panel:-:Pt:Plas.cfDNA:-:Sequencing

Preferred Label : Noninvasive prenatal fetal 18 & 21 aneuploidy panel:-:Pt:Plas.cfDNA:-:Sequencing;

LOINC status : ACTIVE;

LOINC display name : Noninvasive prenatal fetal 18 and 21 aneuploidy panel Sequencing (cfDNA);

LOINC long common name : Noninvasive prenatal fetal 18 and 21 aneuploidy panel - Plasma cell-free DNA by Sequencing;

LOINC short name : NIP fet 18 21 aneu pnl Plas.cfDNA Seq;

LOINC description : This term was created for, but is not limited in use to, Sequenom Laboratories' VisibiliT panel, which analyzes circulating cell-free DNA extracted from maternal plasma using whole genome sequencing to determine the risk for fetal chromosome 18 and 21 aneuploidies. VisibiliT is indicated for use in pregnant women with average risk for fetal chromosomal aneuploidy.;

Details

Origin ID

77019-8;

UMLS CUI

C4037265;

Has component
- Noninvasive prenatal fetal 18 and 21 aneuploidy panel [LOINC component]
Has method
- Sequencing [LOINC method]
Has system
- Plasma [LOINC System]
- Plasma cell-free DNA [LOINC System]
- cell free DNA [LOINC System]
Has time aspect
- Point in time (spot) [LOINC time aspect]
Panel of LOINC codes
- Fetal trisomy 18 risk:Imp:Pt:Plas.cfDNA:Ord:Sequencing [LOINC code]
- Fetal trisomy 21 risk:Imp:Pt:Plas.cfDNA:Ord:Sequencing [LOINC code]
Semantic type(s)
- Clinical Attribute [UMLS semantic type]

Keyword's position in hierarchy(ies) :

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