Fetal 22q11.2 deletion risk:Imp:Pt:Plas.cfDNA:Ord:Dosage of chromosome specific cf
DNA - CISMeF
Fetal 22q11.2 deletion risk:Imp:Pt:Plas.cfDNA:Ord:Dosage of chromosome specific cf
DNALOINC code
Preferred Label : Fetal 22q11.2 deletion risk:Imp:Pt:Plas.cfDNA:Ord:Dosage of chromosome specific cf
DNA;
LOINC status : ACTIVE;
LOINC display name : 22q11.2 del risk Dosage of chromosome-specific cfDNA Ql (cfDNA) [Interp];
LOINC long common name : Fetal 22q11.2 deletion risk [Interpretation] based on Plasma cell-free DNA by Dosage
of chromosome-specific cfDNA Qualitative;
LOINC short name : Fet 22q11.2 del risk Plas.cfDNA Ql;
LOINC description : The ordinal risk interpretation (e.g. high risk/low risk or high probability/low probability)
of the fetus having a 22q11.2 deletion based on dosage of chromosome specific cell-free
DNA (cf DNA) in maternal plasma that contains both fetal and maternal DNA. Results
may also be based on the mother's current age, IVF status (self, non-self, or not
applicable), and gestational age. This code is based, but not limited in use to, the
submitter's test, the Harmony Prenatal Test, a non-invasive prenatal test for screening
of fetal aneuploidy as well as the 22q11.2 deletion.;