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Status Information

Status
TRIAL

Term Description

The chromosome region where the structural variant was found, for example, 17p12. This term may be used when more specific information, such as the structural variant reported start-end LOINC 81287-5, precision of boundaries LOINC 81288-3 and inner and outer start-end LOINC 81302-2 and LOINC 81301-4, respectively, cannot be or are not reported.

LOINC Names Get Info

Fully-Specified Name
Structural variant cytogenetic location:ID:Pt:^Patient:Nom:
Long Common Name
Structural variant cytogenetic location [Identifier]
Short Name
Struct var cyto loc ID
Display Name
Structural variant cytogenetic location Nom [ID]
Consumer Name Alpha Get Info
Structural variant cytogenetic location

Part Model Get Info

  • Component
    Structural variant cytogenetic location
    LP212314-1
    • Analyte
      Structural variant cytogenetic location
      LP212314-1
      • Component Numerator
        Structural variant cytogenetic location
        LP212314-1
        • Component Numerator Core
          Structural variant cytogenetic location
          LP212314-1
        • Component Numerator Core Suffix
          NULL
           
      • Component Denominator
        NULL
         
        • Component Denominator Core
          NULL
           
        • Component Denominator Core Suffix
          NULL
           
    • Challenge
      NULL
       
    • Adjustment
      NULL
       
    • Count
      NULL
       
  • Property
    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 2.56 (ADD)
Order vs. Observation
Observation

Language Variants Get Info

TagLanguageTranslation
cs-CZCzech (Czechia)Strukturální varianta cytogenetická lokalizace:Identifikátor:Časový bod:^Pacient:Nominální:
el-GRGreek (Greece)Κυτταρογενετική θέση δομικής παραλλαγής:Αναγνωριστικό:Pt:^Ασθενής:Nom:
Synonyms: - MOLPATH Nom Pt Αναγνωριστικό Ασθενής Δομική παραλλαγή Κυτταρογενετική θέση δομικής παραλλαγής
es-ESSpanish (Spain)Ubicación citogenética variante estructural:Código identificador:Punto temporal:^paciente:Nom:
es-MXSpanish (Mexico)Ubicación citogenética de variantes estructurales:Identificador:Punto temporal:^ Paciente:Nominal:
fr-FRFrench (France)Variant structurel Localisation cytogénétique:Identifiant:Ponctuel:^patient:Résultat nominal:
it-ITItalian (Italy)Localizzazione della variante strutturale citogenetica:ID:Pt:^Paziente:Nom:
Synonyms: Identificatore Patologia molecolare paziente Punto nel tempo (episodio)
pl-PLPolish (Poland)Cytogenetyczna lokalizacja wariantu strukturalnego:identyfikator:punkt w czasie:^pacjent:skala nominalna:
Synonyms: wynik kategorialny
zh-CNChinese (China)结构变异细胞遗传学位置: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 地点;场所;部位;定位;地方 时刻;随机;随意;瞬间 标识;身份标识符;身份标识 结构性变异;结构性遗传性变异（遗传变异、基因变异、传性变型、遗传变异体、基因变异体） 结构性变异细胞遗传学位置;结构性遗传性变异（遗传变异、基因变异、传性变型、遗传变异体、基因变异体）细胞遗传学位置

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

CodeSystem lookup
https://fhir.loinc.org/CodeSystem/$lookup?system=http://loinc.org&code=81298-2