Fetal chromosome 13 trisomy:PrThr:Pt:Plas.cfDNA:Ord:Sequencing

Preferred Label : Fetal chromosome 13 trisomy:PrThr:Pt:Plas.cfDNA:Ord:Sequencing;

LOINC status : ACTIVE;

LOINC display name : Chr 13 trisomy Sequencing Ql (cfDNA);

LOINC long common name : Fetal Chromosome 13 trisomy [Presence] based on Plasma cell-free DNA by Sequencing;

LOINC short name : Fet Chr 13 Ts Plas.cfDNA Ql;

LOINC description : This term was created for, but is not limited in use to, Sequenom Laboratories' MaterniT21 PLUS trisomy 13 test, which analyzes circulating cell-free DNA extracted from maternal plasma for chromosome 13 aneuploidy using whole genome sequencing. MaterniT21 PLUS is indicated for use in pregnant women with increased risk for fetal chromosomal aneuploidy.;

Details

Origin ID

77013-1;

UMLS CUI

C4019186;

Has component
- Chromosome [LOINC component]
- Fetal chromosome 13 trisomy [LOINC component]
Has method
- Sequencing [LOINC method]
Has property
- Presence or Threshold [LOINC Property]
Has scale
- Ord [LOINC scale]
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]
Part of panel
- Noninvasive prenatal fetal 13 & 18 & 21 aneuploidy panel:-:Pt:Plas.cfDNA:-:Sequencing [LOINC code]
- Noninvasive prenatal fetal aneuploidy and microdeletion panel:-:Pt:Plas.cfDNA:-:Sequencing [LOINC code]
Semantic type(s)
- Clinical Attribute [UMLS semantic type]

Keyword's position in hierarchy(ies) :

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