75560-3
Fetal Trisomy 21 prior risk [Likelihood] Based on maternal age
Active
Part Description
LP185800-2 Based on maternal age
The fetal risk for having certain disorders, such as Trisomy 21, varies based on maternal age. For such disorders, an individual infant's risk can be estimated based on known population statistics for how many women in a particular age group have an infant born with the condition compared to the total number of pregnancies for that age group. For example, the fetal Trisomy 21 risk is 1 out of 1,000 for a maternal age of 30 and 1 out of 100 for a maternal age of 40.
Source: Regenstrief LOINC
LOINC Names Get Info
- Fully-Specified Name
- Trisomy 21 prior risk:
Likelihood: Pt: ^Fetus: Qn: Based on maternal age - Long Common Name
- Fetal Trisomy 21 prior risk [Likelihood] Based on maternal age
- Short Name
- Fet Ts 21 prior risk from Mat age
- Display Name
- Trisomy 21 prior risk Based on maternal age Qn (fetus)
- Consumer Name Alpha Get Info
- Fetal Trisomy 21 prior risk
Part Model Get Info
- Component
- Trisomy 21 prior risk
LP186092-5
- Analyte
- Trisomy 21 prior risk
LP186092-5
- Component Numerator
- Trisomy 21 prior risk
LP186092-5
- Component Numerator Core
- Trisomy 21 prior risk
LP186092-5
- Component Numerator Core Suffix
- NULL
- Component Denominator
- NULL
- Component Denominator Core
- NULL
- Component Denominator Core Suffix
- NULL
- Challenge
- NULL
- Adjustment
- NULL
- Count
- NULL
- Property
- Likelihood
LP185777-2
- Time
- Pt
LP6960-1
- Time Core
- Pt
LP6960-1
- Time Modifier
- NULL
- System
- ^Fetus
LP310004-9
- System Core
- NULL
- Super System
- Fetus
LP6982-5
- Scale
- Qn
LP7753-9
- Method
- Based on maternal age
LP185800-2
Basic Attributes
- Class
- MOLPATH.TRISOMY
- Type
- Laboratory
- First Released
- Version 2.50
- Last Updated
- Version 2.73 (MIN)
- 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 21 předtestové riziko: |
| el-GR | Greek (Greece) | Προηγούμενος κίνδυνος τρισωμίας 21: Synonyms: - MOLPATH MOLPATH.TRISOMY Pt Qn Έμβρυο Με βάση την ηλικία της μητέρας Πιθανότητα Προηγούμενος κίνδυνος τρισωμίας 21 Τρισωμία 21 |
| es-ES | Spanish (Spain) | Riesgo previo de Trisomía 21: Synonyms: Cuantitativo |
| es-MX | Spanish (Mexico) | Riesgo previo de trisomía 21: |
| fr-FR | French (France) | Risque prédominant trisomie 21: |
| it-IT | Italian (Italy) | Trisomia 21, rischio preesistente: Synonyms: Patologia molecolare Punto nel tempo (episodio) Rischio preesistente di trisomia 21 Trisomia cromosoma genetica |
| pl-PL | Polish (Poland) | Trisomia 21 - ryzyko wstępne: |
| zh-CN | Chinese (China) | 三体型 21 先验风险: Synonyms: 21 三体型综合征(唐氏综合征、 |
Example Units
| Unit | Source |
|---|---|
| {risk} | Example UCUM Units |
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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://