Preferred Label : Fetal chromosome X & Y aneuploidy:Find:Pt:Plas.cfDNA:Nom:Dosage of chromosome specific
cf DNA;
LOINC status : ACTIVE;
LOINC display name : Chr X and Y aneuploidy Dosage of chromosome-specific cfDNA Nom (cfDNA);
LOINC long common name : Chromosome X and Y aneuploidy in Plasma cell-free DNA by Dosage of chromosome-specific
cfDNA Nominal;
LOINC short name : Chr X Y aneup Plas.cfDNA;
LOINC description : Sex chromosome (X & Y) analysis to determine gender (XY or XX) or presence of aneuploidy
can be determined based on dosage of chromosome specific ccf DNA in maternal plasma,
the mother's current age and gestational age. The ccf DNA includes both fetal and
maternal DNA. This code is based, but not limited in use to, the submitter's test,
Harmony Prenatal Test, which is a non-invasive prenatal test intended to aid in the
risk determination of fetal aneuploidy as well as trisomy 13, 18 and 21 in women with
singleton pregnancies of at least 10 weeks gestational age. The submitter's lab reports
results as male fetus, female fetus, or aneuploidy. For aneuploidy cases, the results
of the specific findings (e.g. YY, XYY, XXX, etc.) are reported as well.;
Origin ID : 73822-9;
UMLS CUI : C3654207;
Has component
- Has method
- Has property
- Has scale
- Has system
- Has time aspect
- Part of panel
- Semantic type(s)
