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Term Description

This panel is a subset of the Virtual Medical Record for Clinical Decision Support panel LOINC 74028-2. It contains elements of the disease of interest, whether or not it is present and/or the cause of death in a family member, the family member's estimated age, and the genetic loci (gene identifier) of interest. This panel was created for, but not limited in use to, the Clinical Genomic Choice section in the HL7 v2 Implementation Guide for Virtual Medical Record (VMR). Note that VMR guide is different from the US Surgeon General family health portrait LOINC 54127-6, which is a public tool for users to document and share their family health history information.

Panel Hierarchy

Details for each LOINC in Panel LHC-Forms

LOINCNameR/O/CCardinalityExample UCUM Units
74042-3Genetic diseases history panel Family member HL7.VMR-CDS0..*
Indent74023-3Disease of interest in family member
Indent74022-5Negative history for disease of interest in family member
Indent74044-9Disease of interest was cause of death in family member
Indent21611-9Age estimateda
Indent48018-6Gene studied [ID]

Question Cardinality

0..*

LOINC Names Get Info

Fully-Specified Name
Genetic diseases history panel:-:Pt:^Family member:-:HL7.VMR-CDS
Long Common Name
Genetic diseases history panel Family member HL7.VMR-CDS
Short Name
Genetic diseases hx Pnl Fam Mem VMR-CDS

Part Model Get Info

  • Component
    Genetic diseases history panel
    LP173662-0
    • Analyte
      Genetic diseases history panel
      LP173662-0
      • Component Numerator
        Genetic diseases history panel
        LP173662-0
        • Component Numerator Core
          Genetic diseases history panel
          LP173662-0
        • Component Numerator Core Suffix
          NULL
           
      • Component Denominator
        NULL
         
        • Component Denominator Core
          NULL
           
        • Component Denominator Core Suffix
          NULL
           
    • Challenge
      NULL
       
    • Adjustment
      NULL
       
    • Count
      NULL
       
  • Property
    -
    LP6769-6
  • Time
    Pt
    LP6960-1
  • System
    ^Family member
    LP281750-2
    • System Core
      NULL
       
    • Super System
      Family member
      LP6981-7
  • Scale
    -
    LP7747-1
  • Method
    HL7.VMR-CDS
    LP173568-9

Basic Attributes

Class
PANEL.CLIN
Type
Clinical
First Released
Version 2.46
Last Updated
Version 2.48 (MIN)
Order vs. Observation
Subset
Panel Type
Panel

Member of these Panels

LOINCLong Common Name
74028-2Virtual Medical Record for Clinical Decision Support panel HL7.VMR-CDS

Language Variants Get Info

TagLanguageTranslation
el-GRGreek (Greece)Πίνακας ιστορικού γενετικών νόσων:-:Pt:^Μέλος οικογένειας:-:HL7.VMR-CDS
Synonyms: - CLIN HL7.VMR-CDS PANEL.CLIN Pt Γενετικές ασθένειες Μέλος οικογένειας Οικογένεια Πίνακας ιστορικού γενετικών νόσων
es-MXSpanish (Mexico)Panel de historia de enfermedades genéticas:-:Punto temporal:^ Miembro de la familia:-:HL7.VMR-CDS
it-ITItalian (Italy)Anamnesi malattie genetiche, panel:-:Pt:^membro della famiglia:-:HL7.VMR-CDS
Synonyms: Clinico HL7 Virtual Medical Record for Clinical Decision S Panel anamnesi malattie genetiche Punto nel tempo (episodio) Set clinico NEC (non classificato altrove)
zh-CNChinese (China)遗传性疾病史组套:-:时间点:^家族成员:-:HL7.VMR-CDS
Synonyms: HL7针对临床决策支持的虚拟病历;HL7针对CDS的VMR;HL7 Virtual Medical Record for Clinical Decision Support 医嘱套餐 医嘱套餐类 医嘱套餐组 医嘱组 医嘱组.临床;组套（组合、医嘱组、套餐、套餐医嘱、医嘱套餐、组合申请、组合项目）.临床（CLIN、Clinical） 医嘱组合 医嘱组合类 医嘱组套 医嘱组套类 医嘱组类 多重;多重型;多重标尺类型;多重精度类型 套餐 套餐医嘱 套餐医嘱组 套餐医嘱组类 实验室医嘱套餐 实验室医嘱套餐类 实验室医嘱组 实验室医嘱组合类 实验室医嘱组套 实验室医嘱组套类 实验室套餐医嘱组 实验室套餐医嘱组类 实验室检验项目医嘱组合类 实验室检验项目组合类 家人;家庭成员;超系统 - 家庭成员;超系统 - 家族成员 家庭 时刻;随机;随意;瞬间 检验医嘱组合类 检验项目医嘱组合类 检验项目组合类 疾病历史医嘱组;疾病史组套;疾病史组合 组 组合 组合医嘱 组合类 组套 遗传性疾病（遗传疾病、遗传病、基因疾病）史（病史、历史）组套（组合、医嘱组、套餐、套餐医嘱、医嘱套餐、组合申请、组合项目）;遗传疾病史医嘱组;遗传病史医嘱组;遗传病病史医嘱组;基因疾病史医嘱组;遗传性疾病历史医嘱组;遗传性疾病病史医嘱组 遗传疾病;遗传病;基因疾病

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

CodeSystem lookup
https://fhir.loinc.org/CodeSystem/$lookup?system=http://loinc.org&code=74042-3