Plasma cell-free WBC DNA

Preferred Label : Plasma cell-free WBC DNA;

LOINC status : ACTIVE;

LOINC short name : WBC.DNA Plas.cfDNA;

Details

Origin ID

LP185797-0;

UMLS CUI

C3870592;

LOINC code(s)
- Comment on fetal 1p36 deletion risk:Txt:Pt:WBC.DNA+Plas.cfDNA:Nar:Dosage of chromosome specific cf DNA [LOINC code]
- Comment on fetal 22q11.2 deletion risk:Txt:Pt:WBC.DNA+Plas.cfDNA:Nar:Dosage of chromosome specific cf DNA [LOINC code]
- Comment on fetal 5p deletion risk:Txt:Pt:WBC.DNA+Plas.cfDNA:Nar:Dosage of chromosome specific cf DNA [LOINC code]
- Comment on fetal Angelman syndrome risk:Txt:Pt:WBC.DNA+Plas.cfDNA:Nar:Dosage of chromosome specific cf DNA [LOINC code]
- Comment on fetal Monosomy X risk:Txt:Pt:WBC.DNA+Plas.cfDNA:Nar:Dosage of chromosome specific cf DNA [LOINC code]
- Comment on fetal Prader-Willi syndrome risk:Txt:Pt:WBC.DNA+Plas.cfDNA:Nar:Dosage of chromosome specific cf DNA [LOINC code]
- Comment on fetal Triploidy risk:Imp:Pt:WBC.DNA+Plas.cfDNA:Nar:Dosage of chromosome specific cf DNA [LOINC code]
- Comment on fetal Trisomy 13 risk:Txt:Pt:WBC.DNA+Plas.cfDNA:Nar:Dosage of chromosome specific cf DNA [LOINC code]
- Comment on fetal Trisomy 18 risk:Txt:Pt:WBC.DNA+Plas.cfDNA:Nar:Dosage of chromosome specific cf DNA [LOINC code]
- Comment on fetal Trisomy 21 risk:Txt:Pt:WBC.DNA+Plas.cfDNA:Nar:Dosage of chromosome specific cf DNA [LOINC code]
- Comment on overall fetal aneuploidy risk:Txt:Pt:WBC.DNA+Plas.cfDNA:Nar:Dosage of chromosome specific cf DNA [LOINC code]
- Fetal 1p36 deletion risk:Imp:Pt:WBC.DNA+Plas.cfDNA:Ord:Dosage of chromosome specific cf DNA [LOINC code]
- Fetal 1p36 deletion risk:Likelihood:Pt:WBC.DNA+Plas.cfDNA:Nar:Dosage of chromosome specific cf DNA [LOINC code]
- Fetal 1p36 deletion risk:Likelihood:Pt:WBC.DNA+Plas.cfDNA:Qn:Dosage of chromosome specific cf DNA [LOINC code]
- Fetal 22q11.2 deletion risk:Imp:Pt:WBC.DNA+Plas.cfDNA:Ord:Dosage of chromosome specific cf DNA [LOINC code]
- Fetal 22q11.2 deletion risk:Likelihood:Pt:WBC.DNA+Plas.cfDNA:Nar:Dosage of chromosome specific cf DNA [LOINC code]
- Fetal 22q11.2 deletion risk:Likelihood:Pt:WBC.DNA+Plas.cfDNA:Qn:Dosage of chromosome specific cf DNA [LOINC code]
- Fetal 5p deletion risk:Imp:Pt:WBC.DNA+Plas.cfDNA:Ord:Dosage of chromosome specific cf DNA [LOINC code]
- Fetal 5p deletion risk:Likelihood:Pt:WBC.DNA+Plas.cfDNA:Nar:Dosage of chromosome specific cf DNA [LOINC code]
- Fetal 5p deletion risk:Likelihood:Pt:WBC.DNA+Plas.cfDNA:Qn:Dosage of chromosome specific cf DNA [LOINC code]
- Fetal Angelman syndrome risk:Imp:Pt:WBC.DNA+Plas.cfDNA:Ord:Dosage of chromosome specific cf DNA [LOINC code]
- Fetal Angelman syndrome risk:Likelihood:Pt:WBC.DNA+Plas.cfDNA:Nar:Dosage of chromosome specific cf DNA [LOINC code]
- Fetal Angelman syndrome risk:Likelihood:Pt:WBC.DNA+Plas.cfDNA:Qn:Dosage of chromosome specific cf DNA [LOINC code]
- Fetal Prader-Willi syndrome risk:Imp:Pt:WBC.DNA+Plas.cfDNA:Ord:Dosage of chromosome specific cf DNA [LOINC code]
- Fetal Prader-Willi syndrome risk:Likelihood:Pt:WBC.DNA+Plas.cfDNA:Nar:Dosage of chromosome specific cf DNA [LOINC code]
- Fetal Prader-Willi syndrome risk:Likelihood:Pt:WBC.DNA+Plas.cfDNA:Qn:Dosage of chromosome specific cf DNA [LOINC code]
- Fetal monosomy X risk:Imp:Pt:WBC.DNA+Plas.cfDNA:Ord:Dosage of chromosome specific cf DNA [LOINC code]
- Fetal monosomy X risk:Likelihood:Pt:WBC.DNA+Plas.cfDNA:Nar:Dosage of chromosome specific cf DNA [LOINC code]
- Fetal monosomy X risk:Likelihood:Pt:WBC.DNA+Plas.cfDNA:Qn:Dosage of chromosome specific cf DNA [LOINC code]
- Fetal sex:Find:Pt:WBC.DNA+Plas.cfDNA:Nom:Dosage of chromosome specific cf DNA [LOINC code]
- Fetal triploidy risk:Imp:Pt:WBC.DNA+Plas.cfDNA:Ord:Dosage of chromosome specific cf DNA [LOINC code]
- Fetal trisomy 13 risk:Imp:Pt:WBC.DNA+Plas.cfDNA:Ord:Dosage of chromosome specific cf DNA [LOINC code]
- Fetal trisomy 13 risk:Likelihood:Pt:WBC.DNA+Plas.cfDNA:Nar:Dosage of chromosome specific cf DNA [LOINC code]
- Fetal trisomy 13 risk:Likelihood:Pt:WBC.DNA+Plas.cfDNA:Qn:Dosage of chromosome specific cf DNA [LOINC code]
- Fetal trisomy 13+trisomy 18+triploidy risk:Imp:Pt:WBC.DNA+Plas.cfDNA:Ord:Calculated [LOINC code]
- Fetal trisomy 13+trisomy 18+triploidy risk:Likelihood:Pt:WBC.DNA+Plas.cfDNA:Qn:Calculated [LOINC code]
- Fetal trisomy 18 risk:Imp:Pt:WBC.DNA+Plas.cfDNA:Ord:Dosage of chromosome specific cf DNA [LOINC code]
- Fetal trisomy 18 risk:Likelihood:Pt:WBC.DNA+Plas.cfDNA:Nar:Dosage of chromosome specific cf DNA [LOINC code]
- Fetal trisomy 18 risk:Likelihood:Pt:WBC.DNA+Plas.cfDNA:Qn:Dosage of chromosome specific cf DNA [LOINC code]
- Fetal trisomy 21 risk:Imp:Pt:WBC.DNA+Plas.cfDNA:Ord:Dosage of chromosome specific cf DNA [LOINC code]
- Fetal trisomy 21 risk:Likelihood:Pt:WBC.DNA+Plas.cfDNA:Nar:Dosage of chromosome specific cf DNA [LOINC code]
- Fetal trisomy 21 risk:Likelihood:Pt:WBC.DNA+Plas.cfDNA:Qn:Dosage of chromosome specific cf DNA [LOINC code]
- Noninvasive prenatal fetal aneuploidy & 22q11.2 deletion panel:-:Pt:WBC.DNA+Plas.cfDNA:-:Dosage of chromosome specific cf DNA [LOINC code]
- Noninvasive prenatal fetal aneuploidy and microdeletion panel:-:Pt:WBC.DNA+Plas.cfDNA:-:Dosage of chromosome specific cf DNA [LOINC code]
- Noninvasive prenatal fetal aneuploidy panel:-:Pt:WBC.DNA+Plas.cfDNA:-:Dosage of chromosome specific cf DNA [LOINC code]
Semantic type(s)
- Nucleic Acid, Nucleoside, or Nucleotide [UMLS semantic type]

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