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Part Description

LP185907-5   based on general population risk
The risk of having or developing a specific disorder can be calculated by several different methods. One method uses known statistics for the general population as a whole to estimate a single individual's risk. For example, if 30 cases of a certain genetic condition that presents at birth are diagnosed in one year in a geographic area that has 300,000 live births per year, the individual infant's risk of having this condition is approximately 1 in 10,000 live births. Source: Regenstrief LOINC

LOINC Names Get Info

Fully-Specified Name
Prader-Willi syndrome prior risk:Likelihood:Pt:^Fetus:Qn:Based on general population risk
Long Common Name
Fetal Prader-Willi syndrome prior risk [Likelihood] based on general population risk
Short Name
Fet PWS prior risk from Pop risk
Display Name
Prader-Willi syndrome prior risk based on general population risk Qn (fetus)
Consumer Name Alpha Get Info
Fetal Prader-Willi syndrome prior risk

Part Model Get Info

  • Component
    Prader-Willi syndrome prior risk
    LP185769-9
    • Analyte
      Prader-Willi syndrome prior risk
      LP185769-9
      • Component Numerator
        Prader-Willi syndrome prior risk
        LP185769-9
        • Component Numerator Core
          Prader-Willi syndrome prior risk
          LP185769-9
        • 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
  • System
    ^Fetus
    LP310004-9
    • System Core
      NULL
       
    • Super System
      Fetus
      LP6982-5
  • Scale
    Qn
    LP7753-9
  • Method
    based on general population risk
    LP185907-5

Basic Attributes

Class
MOLPATH.DEL
Type
Laboratory
First Released
Version 2.50
Last Updated
Version 2.73 (MIN)
Order vs. Observation
Both

Member of these Panels

LOINCLong Common Name
75547-0Noninvasive prenatal fetal aneuploidy and microdeletion panel based on Plasma cell-free+WBC DNA by Dosage of chromosome-specific circulating cell free (ccf) DNA

Language Variants Get Info

TagLanguageTranslation
cs-CZCzech (Czechia)Prader-Williho syndrom předtestové riziko:Pravděpodobnost:Časový bod:^Plod:Kvantitativní:Na základě obecného populačního rizika
el-GRGreek (Greece)Προηγούμενος κίνδυνος συνδρόμου Prader-Willi:Πιθανότητα:Pt:^Έμβρυο:Qn:με βάση τον γενικό κίνδυνο πληθυσμού
Synonyms: - MOLPATH MOLPATH.DEL Pt Qn Έμβρυο με βάση τον γενικό κίνδυνο πληθυσμού Πιθανότητα Προηγούμενος κίνδυνος συνδρόμου Prader-Willi
es-ESSpanish (Spain)Riesgo previo de síndrome de Prader-Willi:Probabilidad:Punto temporal:^Feto:Qn:Basado en el riesgo de la población general
Synonyms: Cuantitativo
es-MXSpanish (Mexico)Riesgo previo del síndrome de Prader-Willi:Probabilidad:Punto temporal:^ Feto:Cuantitativo:basado en el riesgo de la población general
fr-FRFrench (France)Risque prédominant syndrome de Prader-Willi:Probabilité:Ponctuel:^foetus:Numérique:Basé sur le risque pour la population
it-ITItalian (Italy)Sindrome di Prader Willi, rischio preesistente:Probabilità:Pt:^feto:Qn:basato sul rischio nella popolazione generale
Synonyms: Delezione genetica Patologia molecolare Punto nel tempo (episodio) Rischio preesistente di sindrome di Prader Willi
zh-CNChinese (China)普拉德-威利综合征先验风险:似然性:时间点:^胎儿:定量型:基于一般人群风险的方法
Synonyms: 分子病理学.基因缺失;分子病理学.缺失;分子病理学试验.基因缺失;分子病理学试验.缺失;分子病理学试验类.缺失;基因缺失;缺失 分子病理学;分子病理学试验 可用数量表示的;定量性;数值型;数量型;连续数值型标尺 可能性;似然;可能 基于一般（普通）人群风险的方法 时刻;随机;随意;瞬间 普拉德-威利综合征先验风险（事前风险、事先风险）;Prader-Willi 综合征先验风险（危险性、风险性、危险）;小胖威利症候群先验风险;普瑞德威利症候群先验风险;普瑞德威利氏症候群先验风险;普拉德威利症候群先验风险 胎;超系统 - 胎儿

Example Units

UnitSource
{risk}Example UCUM Units

LOINC Terminology Service (API) using HL7® FHIR® Get Info

CodeSystem lookup
https://fhir.loinc.org/CodeSystem/$lookup?system=http://loinc.org&code=75580-1