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Status Information

Status
TRIAL

Term Description

This term is used to report the unique identifier of the complex variant found in this study. The identifier may come from various sources, including NCBI's ClinVar and Ensembl. For example, the variant NM_000106.5(CYP2D6):c.[886C>T;457G>C] - Haplotype has the ClinVar ID 16895. http://www.ncbi.nlm.nih.gov/clinvar/variation/16895/

LOINC Names Get Info

Fully-Specified Name
Complex variant:ID:Pt:^Patient:Nom:
Long Common Name
Complex genetic variant [ID]
Short Name
Comp var ID
Display Name
Complex variant Nom [ID]
Consumer Name Alpha Get Info
Complex variant

Part Model Get Info

  • Component
    Complex variant
    LP212306-7
    • Analyte
      Complex variant
      LP212306-7
      • Component Numerator
        Complex variant
        LP212306-7
        • Component Numerator Core
          Complex variant
          LP212306-7
        • Component Numerator Core Suffix
          NULL
           
      • Component Denominator
        NULL
         
        • Component Denominator Core
          NULL
           
        • Component Denominator Core Suffix
          NULL
           
    • Challenge
      NULL
       
    • Adjustment
      NULL
       
    • Count
      NULL
       
  • Property
    ID
    LP6818-1
  • Time
    Pt
    LP6960-1
  • System
    ^Patient
    LP310005-6
    • System Core
      NULL
       
    • Super System
      Patient
      LP6985-8
  • Scale
    Nom
    LP7750-5
  • Method
    NULL
     

Basic Attributes

Class
MOLPATH
Type
Laboratory
First Released
Version 2.56
Last Updated
Version 2.58 (MIN)
Order vs. Observation
Observation

Member of these Panels

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

Language Variants Get Info

TagLanguageTranslation
cs-CZCzech (Czechia)Komplexní varianta:Identifikátor:Časový bod:^Pacient:Nominální:
el-GRGreek (Greece)Σύνθετη παραλλαγή:Αναγνωριστικό:Pt:^Ασθενής:Nom:
Synonyms: - MOLPATH Nom Pt Αναγνωριστικό Ασθενής Σύνθετη παραλλαγή
es-ESSpanish (Spain)Variante compleja:Código identificador:Punto temporal:^paciente:Nom:
es-MXSpanish (Mexico)Variante compleja:Identificador:Punto temporal:^ Paciente:Nominal:
fr-FRFrench (France)Variant complexe:Identifiant:Ponctuel:^patient:Résultat nominal:
it-ITItalian (Italy)Variante complessa:ID:Pt:^Paziente:Nom:
Synonyms: Identificatore Patologia molecolare paziente Punto nel tempo (episodio)
zh-CNChinese (China)复杂变异:标识符:时间点:^患者:名义型:
Synonyms: 分子病理学;分子病理学试验 分类型应答;分类型结果;名义性;名称型;名词型;名词性;标称性;没有自然次序的名义型或分类型应答 医疗服务对象;客户;病人;病患;病号;超系统 - 病人 复合体 复杂遗传性变异（遗传变异、基因变异、传性变型、遗传变异体、基因变异体） 时刻;随机;随意;瞬间 标识;身份标识符;身份标识

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

CodeSystem lookup
https://fhir.loinc.org/CodeSystem/$lookup?system=http://loinc.org&code=81260-2