Fetal chromosome X & Y aneuploidy risk:Imp:Pt:Plas.cfDNA:Ord:Sequencing

Preferred Label : Fetal chromosome X & Y aneuploidy risk:Imp:Pt:Plas.cfDNA:Ord:Sequencing;

LOINC status : ACTIVE;

LOINC display name : Chr X and Y aneuploidy risk Sequencing Ql (cfDNA) [Interp];

LOINC long common name : Fetal Chromosome X and Y aneuploidy risk [interpretation] in Plasma cell-free DNA Qualitative by Sequencing;

LOINC short name : Fet X Y aneup risk Plas.cfDNA Seq-Imp;

LOINC description : The risk interpretation (e.g. increased risk) of chromosome X & Y aneuploidy present in fetal cell-free DNA from maternal plasma. This term was created for, but not limited in use to, QNatal Advanced, a non-invasive prenatal test which uses massively parallel sequencing to identify chromosome X & Y aneuploidy.;

Details

Origin ID

79211-9;

UMLS CUI

C4070376;

Has component
- Chromosome [LOINC component]
- Chromosome X and Y aneuploidy [LOINC component]
- Fetal Chromosome X and Y aneuploidy risk [LOINC component]
- Fetal chromosome X and Y aneuploidy [LOINC component]
Has method
- Sequencing [LOINC method]
Has property
- Impression/interpretation of study [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]
Semantic type(s)
- Clinical Attribute [UMLS semantic type]

Keyword's position in hierarchy(ies) :

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