75558-7
Fetal Trisomy 18 risk [Interpretation] based on Plasma cell-free+WBC DNA by Dosage of chromosome-specific cfDNA Qualitative
Active
Term Description
This term was developed for, but is not limited in use to, Natera's Panorama noninvasive prenatal test for fetal aneuploidies and microdeletions.
LOINC Names Get Info
- Fully-Specified Name
- Fetal trisomy 18 risk:
Imp: Pt: WBC.DNA+Plas.cfDNA: Ord: Dosage of chromosome specific cf DNA - Long Common Name
- Fetal Trisomy 18 risk [Interpretation] based on Plasma cell-free+WBC DNA by Dosage of chromosome-specific cfDNA Qualitative
- Short Name
- Fet Ts 18 risk WBC.DNA+cfDNA Ql
- Display Name
- Trisomy 18 risk Dosage of chromosome-specific cfDNA Ql (Plasma cell-free+WBC DNA) [Interp]
- Consumer Name Alpha Get Info
- Fetal Trisomy 18 risk
Part Model Get Info
- Component
- Fetal trisomy 18 risk
LP410749-8
- Analyte
- Fetal trisomy 18 risk
LP410749-8
- Component Numerator
- Fetal trisomy 18 risk
LP410749-8
- Component Numerator Core
- Fetal trisomy 18 risk
LP410749-8
- 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
- WBC.DNA+Plas.cfDNA
LP185797-0
- System Core
- WBC.DNA+Plas.cfDNA
LP185797-0
- Super System
- NULL
- Scale
- Ord
LP7751-3
- Method
- Dosage of chromosome specific cf DNA
LP172871-8
Example Answer List: LL3000-8
Source: Natera| Answer | Code | Score | Answer ID |
|---|---|---|---|
| Low risk | LA19542-2 | ||
| High risk | LA19541-4 | ||
| Risk unchanged | LA21393-6 | ||
| Test not performedCopyright http://snomed.info/sct ID:262008008 Not performed (qualifier value) | LA13546-9 |
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
- Both
Member of these Panels
| LOINC | Long Common Name |
|---|---|
| 96978-2 | Noninvasive prenatal fetal aneuploidy and 22q11.2 deletion panel - Plasma cell-free+WBC DNA by Dosage of chromosome-specific cfDNA |
| 75547-0 | Noninvasive prenatal fetal aneuploidy and microdeletion panel based on Plasma cell-free+WBC DNA by Dosage of chromosome-specific circulating cell free (ccf) DNA |
| 96977-4 | Noninvasive prenatal fetal aneuploidy panel - Plasma cell-free+WBC DNA by Dosage of chromosome-specific cfDNA |
Language Variants Get Info
| Tag | Language | Translation |
|---|---|---|
| cs-CZ | Czech (Czechia) | Trizomie 18 riziko u plodu: |
| el-GR | Greek (Greece) | Κίνδυνος εμβρυϊκής τρισωμίας 18: Synonyms: Imp MOLPATH MOLPATH.TRISOMY Ord Pt Αριθμός λευκών αιμοσφαιρίων Αριθμός λευκών αιμοσφαιρίων.DNA+Πλάσμα.cfDNA Δοσολογία ειδικού χρωμοσωμικού cf DNA Κίνδυνος εμβρυϊκής τρισωμίας 18 Κίνδυνος τρισωμίας 18 Πλάσμα Πλάσμα.cfDNA |
| es-ES | Spanish (Spain) | Riesgo de trisomía 18 fetal: |
| es-MX | Spanish (Mexico) | Riesgo de trisomía 18 fetal: |
| fr-FR | French (France) | Risque de trisomie 18 foetale: |
| it-IT | Italian (Italy) | Trisomia 18, rischio: Synonyms: DNA libero circolante nel plasma Dosaggio di DNA libero fetale circolante cromosoma Globuli bianchi Globuli bianchi+DNA libero circolante nel plasma Impressione/interpretazione di studio Patologia molecolare Plasma Punto nel tempo (episodio) Rischio di trisomia 18 Trisomia cromosoma genetica |
| pl-PL | Polish (Poland) | Ryzyko trisomii 18 u płodu: Synonyms: DNA leukocytów i wolnokrążące DNA w osoczu Ryzyko trisomii chromosomu 18 u płodu wolnokrążące DNA w osoczu |
| zh-CN | Chinese (China) | 胎儿三体型 18 风险: Synonyms: 18 三体型综合征风险(危险性、 |
LOINC Terminology Service (API) using HL7® FHIR® Get Info
Requests to this service require a free LOINC username and password. Below is a sample of the possible capabilities. See the LOINC Terminology Service documentation for more information.
Third Party Copyright
This material includes SNOMED Clinical Terms® (SNOMED CT®) which is used by permission of the International Health Terminology Standards Development Organisation (IHTSDO) under license. All rights reserved. SNOMED CT® was originally created by The College of American Pathologists. "SNOMED" and "SNOMED CT" are registered trademarks of the IHTSDO.
This material includes content from the US Edition to SNOMED CT, which is developed and maintained by the U.S. National Library of Medicine and is available to authorized UMLS Metathesaurus Licensees from the UTS Downloads site at https://uts.nlm.nih.gov.
Use of SNOMED CT content is subject to the terms and conditions set forth in the SNOMED CT Affiliate License Agreement. It is the responsibility of those implementing this product to ensure they are appropriately licensed and for more information on the license, including how to register as an Affiliate Licensee, please refer to https://www.snomed.org/get-snomed or [email protected]<mailto:[email protected]>. This may incur a fee in SNOMED International non-Member countries.
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://