Chorionic villus sample

Preferred Label : Chorionic villus sample;

LOINC status : ACTIVE;

LOINC short name : CVS;

Synonyme UMLS : CVB - Chorionic villus biopsy; CVS - Chorionic villus sampling; Sampling of chorionic villus; Chorionic Villi Sampling; biopsy chorionic villous;

Details

Origin ID

LP30806-1;

UMLS CUI

C0008509;

Automatic exact mappings (from CISMeF team)
- Biopsy chorionic villous [MedDRA Preferred Term]
- Chorionic Villus [NCIt concept]
- Chorionic Villus Sampling [NCIt concept]
- Chorionic villi specimen (specimen) [SNOMED CT concept]
- Chorionic villus sampling [ICHI intervention]
- Entire cardiovascular system (body structure) [SNOMED CT concept]
- Primary Chorionic Villus [NCIt concept]
- Sampling of chorionic villus (procedure) [SNOMED CT concept]
- chorionic villi [MeSH Descriptor]
- chorionic villi [MeSH concept]
- chorionic villi sampling [MeSH Descriptor]
- chorionic villi sampling [MeSH concept]
- chorionic villus [Radlex concept]
- prenatal testing [MedlinePlus Topic]
False automatic mappings
- Cabo Verde [NCIt concept]
- Coefficient of Variance [NCIt concept]
- Curriculum Vitae [NCIt concept]
- Cyclophosphamide/Etoposide Regimen [NCIt concept]
- Human coronavirus sensitivity [OMIM Phenotype]
- Schedule V Substance [NCIt concept]
- Supper [NCIt concept]
LOINC code(s)
- Adenine phosphoribosyltransferase:CCnt:Pt:CVS:Qn: [LOINC code]
- Adenosine deaminase:CCnt:Pt:CVS:Qn: [LOINC code]
- Argininosuccinate lyase:CCnt:Pt:CVS:Qn: [LOINC code]
- Argininosuccinate synthase:CCnt:Pt:CVS:Qn: [LOINC code]
- Carnitine acyltransferase II:CCnt:Pt:CVS:Qn: [LOINC code]
- Carnitine palmitoyltransferase 2:CCnt:Pt:CVS:Qn: [LOINC code]
- Cell growth:PrThr:Pt:CVS:Ord:Tissue culture [LOINC code]
- Cells analyzed:Num:Pt:CVS:Qn:Molgen [LOINC code]
- Cells counted:Num:Pt:CVS:Qn:Molgen [LOINC code]
- Cells karyotyped.total:Num:Pt:CVS:Qn: [LOINC code]
- Chromosome 12 aneuploidy:Find:Pt:Amnio fld/CVS:Nom:FISH [LOINC code]
- Chromosome 13 aneuploidy:Find:Pt:Amnio fld/CVS:Nom:FISH [LOINC code]
- Chromosome 13+18+21+X+Y aneuploidy:Find:Pt:Amnio fld/CVS:Nom:FISH [LOINC code]
- Chromosome 18 aneuploidy:Find:Pt:Amnio fld/CVS:Nom:FISH [LOINC code]
- Chromosome 21 aneuploidy:PrThr:Pt:Amnio fld/CVS:Ord:FISH [LOINC code]
- Chromosome X aneuploidy:PrThr:Pt:Amnio fld/CVS:Ord:FISH [LOINC code]
- Chromosome Y aneuploidy:PrThr:Pt:Amnio fld/CVS:Ord:FISH [LOINC code]
- Chromosome analysis panel:-:Pt:CVS:-:G-banded [LOINC code]
- Chromosome analysis.interphase:Imp:Pt:CVS:Nar:FISH [LOINC code]
- Chromosome analysis:Find:Pt:Amnio fld/CVS:Doc:Microarray [LOINC code]
- Chromosome region 15q11-13 deletion+duplication:Find:Pt:Amnio fld/CVS:Doc:FISH [LOINC code]
- Chromosome region 16p13.3 deletion:Find:Pt:Amnio fld/CVS:Doc:FISH [LOINC code]
- Chromosome region 17p11.2 deletion:Find:Pt:Amnio fld/CVS:Doc:FISH [LOINC code]
- Chromosome region 17p13.3 deletion:Find:Pt:Amnio fld/CVS:Doc:FISH [LOINC code]
- Chromosome region 22q11.2 deletion+duplication:Find:Pt:Amnio fld/CVS:Doc:FISH [LOINC code]
- Chromosome region 7q11.23 deletion:Find:Pt:Amnio fld/CVS:Doc:FISH [LOINC code]
- Chromosome uniparental disomy:Prid:Pt:Amnio fld/CVS:Nar:Molgen [LOINC code]
- Cystine:SCnt:Pt:CVS:Qn: [LOINC code]
- DMD gene deletion+duplication:Find:Pt:Amnio fld/CVS:Doc:MLPA [LOINC code]
- F8 gene intron 1 & 22 inversion targeted mutation analysis:Find:Pt:Amnio fld/CVS:Doc:Molgen [LOINC code]
- F8 gene intron 1 inversion targeted mutation analysis:Find:Pt:Amnio fld/CVS:Doc:Molgen [LOINC code]
- F8 gene intron 22 inversion targeted mutation analysis:Find:Pt:Amnio fld/CVS:Doc:Molgen [LOINC code]
- F9 gene mutation analysis limited to known familial mutations:Find:Pt:Amnio fld/CVS:Doc:Molgen [LOINC code]
- FGFR3 gene targeted mutation analysis:Find:Pt:Amnio fld/CVS:Doc:Molgen [LOINC code]
- FGFR3 gene.p.Gly380Arg targeted mutation analysis:Find:Pt:Amnio fld/CVS:Doc:Molgen [LOINC code]
- FXN gene.GAA repeats:PrThr:Pt:Amnio fld/CVS:Ord:Molgen [LOINC code]
- Germline disorder chromosome analysis:Find:Pt:Amnio fld/CVS:Doc:Mate pair sequencing [LOINC code]
- Glutamate dehydrogenase:CCnt:Pt:CVS:Qn: [LOINC code]
- HBA1 & HBA2 gene deletion:Find:Pt:Amnio fld/CVS:Doc:Molgen [LOINC code]
- HBA1 & HBA2 gene full mutation analysis:Find:Pt:Amnio fld/CVS:Doc:Molgen [LOINC code]
- HBB gene full mutation analysis:Find:Pt:Amnio fld/CVS:Doc:Sequencing [LOINC code]
- HTT gene.CAG repeats:PrThr:Pt:Amnio fld/CVS:Ord:Molgen [LOINC code]
- Hypoxanthine phosphoribosyltransferase/Adenine phosphoribosyltransferase:CRto:Pt:CVS:Qn: [LOINC code]
- Hypoxanthine phosphoribosyltransferase:CCnt:Pt:CVS:Qn: [LOINC code]
- IEEE Rosetta cardiovascular panel:-:-:CVS:-: [LOINC code]
- ISCN band level:Num:Pt:CVS:Ord:Molgen [LOINC code]
- KEL gene targeted mutation analysis:Find:Pt:Amnio fld/CVS:Doc:Molgen [LOINC code]
- Karyotype:Prid:Pt:CVS:Nar: [LOINC code]
- Karyotype:Prid:Pt:CVS:Nom: [LOINC code]
- Marker & derivative chromosome analysis:Find:Pt:Amnio fld/CVS:Doc:Cytogenetics [LOINC code]
- Propionyl CO-A carboxylase:CCnt:Pt:CVS:Qn: [LOINC code]
LOINC narrower mappings
- Chorionic villi specimen (specimen) [SNOMED CT concept]
- Chorionic villi structure (body structure) [SNOMED CT concept]
Semantic type(s)
- Diagnostic Procedure [UMLS semantic type]
UMLS correspondences (same concept)
- Biopsy chorionic villous [MedDRA Preferred Term]
- Chorionic Villus Sampling [NCIt concept]
- Sampling of chorionic villus (procedure) [SNOMED CT concept]
- chorionic villi sampling [MeSH concept]
- chorionic villi sampling [MeSH Descriptor]

Keyword's position in hierarchy(ies) :

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