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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
5p deletion prior risk:Likelihood:Pt:^Fetus:Qn:Based on general population risk
Long Common Name
Fetal 5p deletion prior risk [Likelihood] based on general population risk
Short Name
Fet 5p del prior risk from Pop risk
Display Name
5p del prior risk based on general population risk Qn (fetus)
Consumer Name Alpha Get Info
Fetal 5p deletion prior risk

Part Model Get Info

  • Component
    5p deletion prior risk
    LP186095-8
    • Analyte
      5p deletion prior risk
      LP186095-8
      • Component Numerator
        5p deletion prior risk
        LP186095-8
        • Component Numerator Core
          5p deletion prior risk
          LP186095-8
        • Component Numerator Core Suffix
          NULL
           
      • Component Denominator
        NULL
         
        • Component Denominator Core
          NULL
           
        • Component Denominator Core Suffix
          NULL
           
    • Challenge
      NULL
       
    • Adjustment
      NULL
       
    • Count
      NULL
       
  • Property
    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)Oblast 5p delece předtestové riziko:Pravděpodobnost:Časový bod:^Plod:Kvantitativní:Na základě obecného populačního rizika
el-GRGreek (Greece)προηγούμενος κίνδυνος διαγραφής 5p: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 διαγραφής 5p
es-ESSpanish (Spain)Riesgo previo de deleción 5p:Probabilidad:Punto temporal:^Feto:Qn:Basado en el riesgo de la población general
Synonyms: Cuantitativo
es-MXSpanish (Mexico)Riesgo previo de eliminación 5p:Probabilidad:Punto temporal:^ Feto:Cuantitativo:basado en el riesgo de la población general
fr-FRFrench (France)Risque prédominant délétion 5p:Probabilité:Ponctuel:^foetus:Numérique:Basé sur le risque pour la population
it-ITItalian (Italy)Delezione 5p rischio preesistente:Probabilità:Pt:^feto:Qn:basato sul rischio nella popolazione generale
Synonyms: Delezione genetica Patologia molecolare Punto nel tempo (episodio)
pl-PLPolish (Poland)Ryzyko wstępne delecji 5p:prawdopodobieństwo:punkt w czasie:^płód:ilościowy:oparty (-a,-e) na ryzyku w populacji ogólnej
Synonyms: Istniejące wcześniej ryzyko delecji krótkiego ramienia chromosomu 5
zh-CNChinese (China)5p 染色体缺失先验风险:似然性:时间点:^胎儿:定量型:基于一般人群风险的方法
Synonyms: 5p 染色体缺失（基因缺失、缺损、基因缺损、基因删除、删除、基因丢失）先验风险（事前风险、事先风险）;5p 染色体缺失综合征先验风险（危险性、风险性、危险）;染色体 5p 缺失症候群先验风险;5p 染色体缺失综合征;猫叫综合征;猫叫综合症;猫哭症;猫叫症;5p− 综合征;Lejeune 综合征;勒琼综合征;勒琼氏综合征;Cri du chat syndrome;chromosome 5p deletion syndrome;5p− syndrome;Lejeune''s syndrome 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 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=75592-6