Comment on fetal Prader-Willi syndrome risk:Txt:Pt:WBC.DNA Plas.cfDNA:Nar:Dosage of chromosome specific cf DNA

Preferred Label : Comment on fetal Prader-Willi syndrome risk:Txt:Pt:WBC.DNA Plas.cfDNA:Nar:Dosage of chromosome specific cf DNA;

LOINC status : ACTIVE;

LOINC display name : Comment on Prader-Willi syndrome risk Dosage of chromosome-specific cfDNA Nar (Plasma cell-free WBC DNA);

LOINC long common name : Comment on fetal Prader-Willi syndrome risk [Text] in Plasma cell-free WBC DNA by Dosage of chromosome-specific cfDNA Narrative;

LOINC short name : Fet PWS risk comment;

LOINC description : This term was developed for, but is not limited in use to, Natera's Panorama noninvasive prenatal test for fetal aneuploidies and microdeletions.;

Details

Origin ID

75585-0;

UMLS CUI

C3870284;

Has component
- Comment [LOINC component]
- Comment on fetal Prader-Willi syndrome risk [LOINC component]
- Fetal Prader-Willi syndrome risk [LOINC component]
Has method
- Dosage of chromosome-specific cfDNA [LOINC method]
Has property
- Text [LOINC Property]
Has scale
- Nar [LOINC scale]
Has system
- Plasma [LOINC System]
- Plasma cell-free DNA [LOINC System]
- Plasma cell-free+WBC DNA [LOINC System]
- WBC DNA [LOINC System]
- White blood cells [LOINC System]
- cell free DNA [LOINC System]
Has time aspect
- Point in time (spot) [LOINC time aspect]
Part of panel
- Noninvasive prenatal fetal aneuploidy and microdeletion panel:-:Pt:WBC.DNA+Plas.cfDNA:-:Dosage of chromosome specific cf DNA [LOINC code]
Semantic type(s)
- Clinical Attribute [UMLS semantic type]

Keyword's position in hierarchy(ies) :

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