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Status Information

Status
TRIAL

LOINC Names Get Info

Fully-Specified Name
Genetic variation effect on high-risk allele:Imp:Pt:^Patient:Ord:
Long Common Name
Genetic variation's effect on high-risk allele
Short Name
Genetic var eff high-risk allele
Display Name
Genetic variation effect on high-risk allele Ql [Interp]
Consumer Name Alpha Get Info
Genetic variation effect on high-risk allele

Part Model Get Info

  • Component
    Genetic variation effect on high-risk allele
    LP232213-1
    • Analyte
      Genetic variation effect on high-risk allele
      LP232213-1
      • Component Numerator
        Genetic variation effect on high-risk allele
        LP232213-1
        • Component Numerator Core
          Genetic variation effect on high-risk allele
          LP232213-1
        • Component Numerator Core Suffix
          NULL
           
      • Component Denominator
        NULL
         
        • Component Denominator Core
          NULL
           
        • Component Denominator Core Suffix
          NULL
           
    • Challenge
      NULL
       
    • Adjustment
      NULL
       
    • Count
      NULL
       
  • Property
    Imp
    LP6819-9
  • Time
    Pt
    LP6960-1
  • System
    ^Patient
    LP310005-6
    • System Core
      NULL
       
    • Super System
      Patient
      LP6985-8
  • Scale
    Ord
    LP7751-3
  • Method
    NULL
     

Example Answer List: LL2353-2

Source: Regenstrief LOINC
AnswerCodeScoreAnswer ID
Low riskLA19542-2
High riskLA19541-4

Basic Attributes

Class
MOLPATH.PHARMG
Type
Laboratory
First Released
Version 2.58
Last Updated
Version 2.73 (MIN)
Order vs. Observation
Observation
Common Test Rank Get Info
11172

Member of these Panels

LOINCLong Common Name
81247-9Master HL7 genetic variant reporting panel

Language Variants Get Info

TagLanguageTranslation
cs-CZCzech (Czechia)Genetická varianta vliv na vysoce rizikovou alelu:Interpretace:Časový bod:^Pacient:Ordinální:
el-GRGreek (Greece)Επίδραση γενετικών παραλλαγών στο αλληλόμορφο υψηλού κινδύνου:Imp:Pt:^Ασθενής:Ord:
Synonyms: - Imp MOLPATH MOLPATH.PHARMG Ord Pt Ασθενής Επίδραση γενετικών παραλλαγών στο αλληλόμορφο υψηλού κινδύνου
es-ESSpanish (Spain)Efecto de la variación genética en alelo de alto riesgo:Impresión/interpretación del estudio:Punto temporal:^paciente:Ord:
es-MXSpanish (Mexico)Efecto de la variación genética sobre el alelo de alto riesgo:Impresión / interpretación del estudio:Punto temporal:^ Paciente:Ordinal:
fr-FRFrench (France)Effet du polymorphisme génétique sur l'allèle à haut risque:Interprétation:Ponctuel:^patient:Qualitatif:
it-ITItalian (Italy)Variante genetica, effetto sull'allele ad alto rischio:Imp:Pt:^Paziente:Ord:
Synonyms: Effetto della variante genetica sull''allele ad al Farmacogenomica Impressione/interpretazione di studio Patologia molecolare paziente Punto nel tempo (episodio)
pl-PLPolish (Poland)Wpływ zmienności genetycznej na allel wysokiego ryzyka:ocena:punkt w czasie:^pacjent:uporządkowany:
zh-CNChinese (China)遗传性变异对高风险等位基因的影响:印象:时间点:^患者:序数型:
Synonyms: 依次型;分类顺序型;定性的;序数型（或称等级型）;性质上的;有序型;有序性分类应答;有序性分类结果;秩次型;等级型;筛查;顺序型 分子病理学;分子病理学试验 医疗服务对象;客户;病人;病患;病号;超系统 - 病人 印象是一种诊断陈述，始终是对其他某种观察指标的解释或抽象（一系列检验项目结果、一幅图像或者整个某位病人），而且几乎总是由某位专业人员产生。;检查印象;检查印象/解释;检查的印象/解释;检查解释;解释;阐释 时刻;随机;随意;瞬间 遗传性变异（遗传变异、基因变异、传性变型、遗传变异体、基因变异体）对（对于）高风险等位基因的影响（作用）

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

CodeSystem lookup
https://fhir.loinc.org/CodeSystem/$lookup?system=http://loinc.org&code=83009-1