cell free DNA - CISMeF

Preferred Label : cell free DNA;

LOINC status : ACTIVE;

LOINC short name : cfDNA;

Détails

Origin ID

LP158077-0;

UMLS CUI

C4289789;

Automatic exact mappings (from CISMeF team)
- Cell free deoxyribonucleic acid (substance) [SNOMED CT concept]
- Cell-Free Nucleic Acids [MeSH Descriptor]
- Circulating Cell-Free DNA [NCIt concept]
LOINC code(s)
- BRAF gene.p.Val600 mutations:Prid:Pt:Plas.cfDNA:Nom:Molgen [LOINC code]
- Bone marrow transplant chimerism panel:-:Pt:Plas.cfDNA:-:Sequencing [LOINC code]
- Cancer related multigene analysis:Find:Pt:Plas.cfDNA:Doc:Molgen [LOINC code]
- Cell-free DNA.donor/Cell-free DNA.total^post cardiac transplant:NFr:Pt:Plas.cfDNA:Qn: [LOINC code]
- Cell-free DNA.donor/Cell-free DNA.total^post kidney transplant:NFr:Pt:Plas.cfDNA:Qn: [LOINC code]
- Cell-free DNA.donor/Cell-free DNA.total^post lung transplant:NFr:Pt:Plas.cfDNA:Qn: [LOINC code]
- Cell-free DNA.fetal/Cell-free DNA.total:Find:Pt:Plas.cfDNA:Nar:Dosage of chromosome specific cf DNA [LOINC code]
- Cell-free DNA.fetal/Cell-free DNA.total:SFr:Pt:Plas.cfDNA:Qn:Dosage of chromosome specific cf DNA [LOINC code]
- 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]
- EGFR gene.c.2369C>T actual/normal:RelRto:Pt:Plas.cfDNA:Qn:Molgen [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:Plas.cfDNA:Ord: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 RhD antigen:Prid:Pt:Plas.cfDNA:Nom:MS.MALDI-TOF [LOINC code]
- Fetal Y chromosome:Imp:Pt:Plas.cfDNA:Nom:Sequencing [LOINC code]
- Fetal Y chromosome:PrThr:Pt:Plas.cfDNA:Ord:Sequencing [LOINC code]
- Fetal chromosome 13 trisomy:Imp:Pt:Plas.cfDNA:Ord:Dosage of chromosome specific cf DNA [LOINC code]
- Fetal chromosome 13 trisomy:PrThr:Pt:Plas.cfDNA:Ord:Dosage of chromosome specific cf DNA [LOINC code]
- Fetal chromosome 13 trisomy:PrThr:Pt:Plas.cfDNA:Ord:Sequencing [LOINC code]
- Fetal chromosome 13+18+21 trisomy:PrThr:Pt:Plas.cfDNA:Ord:Dosage of chromosome specific cf DNA [LOINC code]
- Fetal chromosome 13+18+21+X+Y aneuploidy:PrThr:Pt:Plas.cfDNA:Ord:Dosage of chromosome specific cf DNA [LOINC code]
- Fetal chromosome 13+18+21+Y aneuploidy:PrThr:Pt:Plas.cfDNA:Ord:Dosage of chromosome specific cf DNA [LOINC code]
- Fetal chromosome 18 trisomy:Imp:Pt:Plas.cfDNA:Ord:Dosage of chromosome specific cf DNA [LOINC code]
- Fetal chromosome 18 trisomy:PrThr:Pt:Plas.cfDNA:Ord:Dosage of chromosome specific cf DNA [LOINC code]
- Fetal chromosome 18 trisomy:PrThr:Pt:Plas.cfDNA:Ord:Sequencing [LOINC code]
- Fetal chromosome 21 trisomy:Imp:Pt:Plas.cfDNA:Ord:Dosage of chromosome specific cf DNA [LOINC code]
- Fetal chromosome 21 trisomy:PrThr:Pt:Plas.cfDNA:Ord:Dosage of chromosome specific cf DNA [LOINC code]
- Fetal chromosome 21 trisomy:PrThr:Pt:Plas.cfDNA:Ord:Sequencing [LOINC code]
- Fetal chromosome X & Y aneuploidy risk:Imp:Pt:Plas.cfDNA:Ord:Sequencing [LOINC code]
- Fetal chromosome X & Y aneuploidy risk:Likelihood:Pt:Plas.cfDNA:Qn:Dosage of chromosome specific cf DNA [LOINC code]
- Fetal chromosome X & Y aneuploidy:Find:Pt:Plas.cfDNA:Nom:Dosage of chromosome specific cf DNA [LOINC code]
- Fetal chromosome X & Y aneuploidy:Imp:Pt:Plas.cfDNA:Nom:Dosage of chromosome specific cf DNA [LOINC code]
- Fetal chromosome X & Y aneuploidy:PrThr:Pt:Plas.cfDNA:Ord:Dosage of chromosome specific cf DNA [LOINC code]
- Fetal chromosome region 11q23 deletion:PrThr:Pt:Plas.cfDNA:Ord:Sequencing [LOINC code]
- Fetal chromosome region 15q11 deletion:PrThr:Pt:Plas.cfDNA:Ord:Sequencing [LOINC code]
- Fetal chromosome region 4p16 deletion:PrThr:Pt:Plas.cfDNA:Ord:Sequencing [LOINC code]
- Fetal chromosome region 8q24 deletion:PrThr:Pt:Plas.cfDNA:Ord:Sequencing [LOINC code]
- Fetal microdeletions risk:Imp:Pt:Plas.cfDNA:Ord:Sequencing [LOINC code]
- Fetal monosomy X risk:Imp:Pt:Plas.cfDNA:Ord: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:Plas.cfDNA:Nom: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 sex:Likelihood:Pt:Plas.cfDNA:Qn: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: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:Plas.cfDNA:Qn: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:Plas.cfDNA:Ord:Dosage of chromosome specific cf DNA [LOINC code]
- Fetal trisomy 18 risk:Imp:Pt:Plas.cfDNA:Ord:Sequencing [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:Plas.cfDNA:Qn: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:Plas.cfDNA:Ord:Dosage of chromosome specific cf DNA [LOINC code]
- Fetal trisomy 21 risk:Imp:Pt:Plas.cfDNA:Ord:Sequencing [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:Plas.cfDNA:Qn: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]
- Kidney transplant acute cellular rejection risk:Score:Pt:Plas.cfDNA:Qn:Calculated.AlloMap [LOINC code]
- Lung cancer screening:PrThr:Pt:Plas.cfDNA:Ord:Sequencing [LOINC code]
- Noninvasive prenatal fetal 13 & 18 & 21 aneuploidy panel:-:Pt:Plas.cfDNA:-:Sequencing [LOINC code]
- Noninvasive prenatal fetal 18 & 21 aneuploidy panel:-:Pt:Plas.cfDNA:-:Sequencing [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:Plas.cfDNA:-:Sequencing [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:Plas.cfDNA:-: [LOINC code]
- Noninvasive prenatal fetal aneuploidy panel:-:Pt:WBC.DNA+Plas.cfDNA:-:Dosage of chromosome specific cf DNA [LOINC code]
- RHD gene allele^fetus:Prid:Pt:Plas.cfDNA:Nom: [LOINC code]
- Single nucleotide polymorphisms.recipient derived cf.dna/Single nucleotide polymorphisms.total cf.dna^ post bone marrow transplant:NFr:Pt:Plas.cfDNA:Qn:Sequencing [LOINC code]
Semantic type(s)
- Biologically Active Substance [UMLS semantic type]
- Nucleic Acid, Nucleoside, or Nucleotide [UMLS semantic type]
UMLS correspondences (same concept)
- Cell free deoxyribonucleic acid (substance) [SNOMED CT concept]
- Circulating Cell-Free DNA [NCIt concept]

Position du mot-clé dans l'(les) arborescence(s) :

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