75559-5
Comment on fetal Trisomy 18 risk [Text] in Plasma cell-free+WBC DNA by Dosage of chromosome-specific cfDNA Narrative
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.
Source: Regenstrief LOINC
Part Descriptions
LP185986-9 Comment on fetal Trisomy 18 risk
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
LP185986-9 Comment on fetal Trisomy 18 risk
The genetic counselor's comment regarding risk of a specific disorder or group of disorders is used to convey follow-up recommendations or other information related to the risk result and interpretation.
Source: Regenstrief LOINC
Fully-Specified Name
- Component
- Comment on fetal Trisomy 18 risk
- Property
- Txt
- Time
- Pt
- System
- WBC.DNA+Plas.cfDNA
- Scale
- Nar
- Method
- Dosage of chromosome specific cf DNA
Additional Names
- Short Name
- Fet Ts 18 risk comment
- Display Name
- Comment on Trisomy 18 risk Dosage of chromosome-specific cfDNA Nar (Plasma cell-free+WBC DNA)
- Consumer Name Alpha Get Info
- Fetal Comment on trisomy 18 risk
Basic Attributes
- Class
- MOLPATH.TRISOMY
- Type
- Laboratory
- First Released
- Version 2.50
- Last Updated
- Version 2.73
- Change Reason
- Release 2.70: COMPONENT: Removed "Genetic counselor" to broaden use since various specialists may provide comments on test results.; Previous Releases: 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 |
---|---|---|
es-ES | Spanish (Spain) | Comentario de consejo genético en riesgo de Trisomía 18: |
es-MX | Spanish (Mexico) | Comentario del consejero genético sobre el riesgo de trisomía 18 fetal: |
fr-FR | French (France) | Risque trisomie 18 foetale (commentaire du conseiller génétique): |
it-IT | Italian (Italy) | Commento su rischio Trisomia 18: Synonyms: DNA libero circolante nel plasma Dosaggio di DNA libero fetale circolante cromosoma Globuli bianchi Globuli bianchi+DNA libero circolante nel plasma Patologia molecolare Plasma Punto nel tempo (episodio) Rischio di trisomia 18 Testo Trisomia cromosoma genetica |
pl-PL | Polish (Poland) | Komentarz dotyczący ryzyka trisomii 18 u płodu: |
zh-CN | Chinese (China) | 关于胎儿三体型 18 风险的遗传咨询师意见: Synonyms: 18 三体型综合征风险(危险性、 |
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