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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
1p36 deletion prior risk:Likelihood:Pt:^Fetus:Nar:Based on general population risk
Long Common Name
Fetal 1p36 deletion prior risk [Likelihood] based on general population risk Narrative
Short Name
Fet 1p36 del prior risk from Pop risk
Display Name
1p36 del prior risk based on general population risk Nar (fetus)
Consumer Name Alpha Get Info
Fetal 1p36 deletion prior risk

Part Model Get Info

  • Component
    1p36 deletion prior risk
    LP185773-1
    • Analyte
      1p36 deletion prior risk
      LP185773-1
      • Component Numerator
        1p36 deletion prior risk
        LP185773-1
        • Component Numerator Core
          1p36 deletion prior risk
          LP185773-1
        • 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
    Nar
    LP7749-7
  • 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 1p36 delece předtestové riziko:Pravděpodobnost:Časový bod:^Plod:Narativní:Na základě obecného populačního rizika
el-GRGreek (Greece)προηγούμενος κίνδυνος διαγραφής 1p36:Πιθανότητα:Pt:^Έμβρυο:Nar:με βάση τον γενικό κίνδυνο πληθυσμού
Synonyms: - MOLPATH MOLPATH.DEL Nar Pt Έμβρυο με βάση τον γενικό κίνδυνο πληθυσμού Πιθανότητα προηγούμενος κίνδυνος διαγραφής 1p36
es-ESSpanish (Spain)Riesgo previo de deleción 1p36:Probabilidad:Punto temporal:^Feto:Narrativo:Basado en el riesgo de la población general
es-MXSpanish (Mexico)Riesgo previo de deleción 1p36:Probabilidad:Punto temporal:^ Feto:Narrativo:basado en el riesgo de la población general
fr-FRFrench (France)Risque prédominant délétion 1p36:Probabilité:Ponctuel:^foetus:Résultat textuel:Basé sur le risque pour la population
it-ITItalian (Italy)Delezione 1p36 rischio preesistente:Probabilità:Pt:^feto:Nar:basato sul rischio nella popolazione generale
Synonyms: Delezione genetica Patologia molecolare Punto nel tempo (episodio)
pl-PLPolish (Poland)Ryzyko wczesnego wystąpienia delecji 1p36:prawdopodobieństwo:punkt w czasie:^płód:opisowy:oparty (-a,-e) na ryzyku w populacji ogólnej
Synonyms: Istniejące wcześniej ryzyko wystąpienia delecji 1p36
zh-CNChinese (China)1p36 染色体缺失先验风险:似然性:时间点:^胎儿:叙述型:基于一般人群风险的方法
Synonyms: 1p36 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）;1p36 染色体缺失综合征先验风险（危险性、风险性、危险）;染色体 1p36 缺失症候群先验风险;1p36 染色体缺失综合征;单体型 1p36;单体性 1p36 单体;1p36;1p36 deletion syndrome;monosomy 1p36 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 叙述;叙述性文字;报告;报告型;文字叙述;文本叙述型;文本描述;文本描述型 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

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

CodeSystem lookup
https://fhir.loinc.org/CodeSystem/$lookup?system=http://loinc.org&code=75599-1