75978-7
Fetal Chromosome 18 trisomy [Interpretation] based on Plasma cell-free DNA by Dosage of chromosome-specific cfDNA Qualitative
Active
Term Description
The interpretation of chromosome 18 aneuploidy (e.g., consistent with diploid, suspected trisomy or consistent with trisomy 18) based on non-invasive prenatal screening methods using cfDNA in maternal plasma.
Part Description
LP187146-8 Fetal chromosome 18 trisomy
Trisomy 18 risk refers to the fetus's risk of having trisomy 18. The risk can be estimated based on maternal age and prenatal genetic testing of fetal DNA.Trisomy 18, also called Edwards syndrome, is caused by the presence of three copies of chromosome 18 in each cell rather than two. Edwards syndrome is associated with intrauterine growth retardation and fetal demise, and liveborn infants with Edwards syndrome typically have low birth weight, congenital heart disease, and characteristic physical features. Less than 10% of liveborn infants with Edwards syndrome live past their first year. The general population risk of Edwards syndrome is 1 out of 5,000 live births, and the risk for Edwards syndrome increases with increasing maternal age. [MedlinePlus Condition: trisomy-18]
Source: Regenstrief LOINC,
GHR: Trisomy 18
LOINC Names Get Info
- Fully-Specified Name
- Fetal chromosome 18 trisomy:
Imp: Pt: Plas.cfDNA: Ord: Dosage of chromosome specific cf DNA - Long Common Name
- Fetal Chromosome 18 trisomy [Interpretation] based on Plasma cell-free DNA by Dosage of chromosome-specific cfDNA Qualitative
- Short Name
- Fet Chr 18 Ts Plas.cfDNA Ql
- Display Name
- Chr 18 trisomy Dosage of chromosome-specific cfDNA Ql (cfDNA) [Interp]
- Consumer Name Alpha Get Info
- Fetal Chromosome 18 trisomy
Part Model Get Info
- Component
- Fetal chromosome 18 trisomy
LP187146-8
- Analyte
- Fetal chromosome 18 trisomy
LP187146-8
- Component Numerator
- Fetal chromosome 18 trisomy
LP187146-8
- Component Numerator Core
- Fetal chromosome 18 trisomy
LP187146-8
- Component Numerator Core Suffix
- NULL
- Component Denominator
- NULL
- Component Denominator Core
- NULL
- Component Denominator Core Suffix
- NULL
- Challenge
- NULL
- Adjustment
- NULL
- Count
- NULL
- Property
- Imp
LP6819-9
- Time
- Pt
LP6960-1
- Time Core
- Pt
LP6960-1
- Time Modifier
- NULL
- System
- Plas.cfDNA
LP185795-4
- System Core
- Plas.cfDNA
LP185795-4
- Super System
- NULL
- Scale
- Ord
LP7751-3
- Method
- Dosage of chromosome specific cf DNA
LP172871-8
Example Answer List: LL3142-8
Source: Laboratory Corporation of America| Answer | Code | Score | Answer ID |
|---|---|---|---|
| Consistent with diploid chromosome 18 | LA21882-8 | ||
| Borderline result suggestive of trisomy 18 | LA21883-6 | ||
| Consistent with trisomy 13 | LA21890-1 |
Basic Attributes
- Class
- MOLPATH.TRISOMY
- Type
- Laboratory
- First Released
- Version 2.50
- Last Updated
- Version 2.73 (MIN)
- Change Reason
- Added "Fetal" to Component to clarify that the result is about the fetus.
- Order vs. Observation
- Observation
- Common Test Rank Get Info
- 7476
Language Variants Get Info
| Tag | Language | Translation |
|---|---|---|
| cs-CZ | Czech (Czechia) | Fetální chromozom 18 trizomie: |
| el-GR | Greek (Greece) | Εμβρυική τρισωμία χρωμοσώματος 18: Synonyms: Imp MOLPATH MOLPATH.TRISOMY Ord Pt Δοσολογία ειδικού χρωμοσωμικού cf DNA Εμβρυική τρισωμία χρωμοσώματος 18 Πλάσμα Πλάσμα.cfDNA Χρωμόσωμα |
| es-ES | Spanish (Spain) | Trisomía cromosoma 18: |
| es-MX | Spanish (Mexico) | Trisomía fetal del cromosoma 18: |
| fr-FR | French (France) | Chromosome 18 trisomie foetale: |
| it-IT | Italian (Italy) | Cromosoma 18, trisomia: Synonyms: DNA libero circolante nel plasma Dosaggio di DNA libero fetale circolante cromosoma Impressione/interpretazione di studio Patologia molecolare Plasma Punto nel tempo (episodio) Trisomia cromosoma genetica Trisomia del cromosoma 18 |
| pl-PL | Polish (Poland) | Trisomia chromosomu 18 u płodu: Synonyms: wolnokrążące DNA w osoczu |
| zh-CN | Chinese (China) | 胎儿染色体 18 三体性: Synonyms: 三体型 三体细胞 三染色体性 三染色体细胞 依次型; |
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LOINC Copyright
Copyright © Regenstrief Institute, Inc. All Rights Reserved. To the extent included herein, the LOINC table and LOINC codes are copyright © Regenstrief Institute, Inc. and the Logical Observation Identifiers Names and Codes (LOINC) Committee. See https://