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Term Description

Multigene testing for heritable breast and gynecological-related germline mutations in genes primarily associated with breast, ovarian, endometrial cancers. Testing is performed to confirm a diagnosis and help guide treatment and management decisions. Identification of a disease-causing variants may also used to inform at-risk relatives. Approximately 5-10 percent of cancers are thought to be hereditary. PMID: 15637391 This test is not appropriate for the detection of somatic mutations in tumor tissue since it is focused on heritable germline mutations.

LOINC Names Get Info

Fully-Specified Name
Hereditary breast & gynecologic cancer multigene analysis:Find:Pt:Bld/Tiss:Doc:Molgen
Long Common Name
Hereditary breast and gynecologic cancer multigene analysis in Blood or Tissue by Molecular genetics method
Short Name
Breast Gyn Multigene Bld/T
Display Name
Hereditary breast and gynecologic cancer multigene analysis Molgen Doc (Bld/Tiss)
Consumer Name Alpha Get Info
Hereditary breast and gynecologic cancer multigene analysis, Blood or tissue specimen

Part Model Get Info

  • Component
    Hereditary breast & gynecologic cancer multigene analysis
    LP426460-4
    • Analyte
      Hereditary breast & gynecologic cancer multigene analysis
      LP426460-4
      • Component Numerator
        Hereditary breast & gynecologic cancer multigene analysis
        LP426460-4
        • Component Numerator Core
          Hereditary breast & gynecologic cancer multigene analysis
          LP426460-4
        • Component Numerator Core Suffix
          NULL
           
      • Component Denominator
        NULL
         
        • Component Denominator Core
          NULL
           
        • Component Denominator Core Suffix
          NULL
           
    • Challenge
      NULL
       
    • Adjustment
      NULL
       
    • Count
      NULL
       
  • Property
    Find
    LP6813-2
  • Time
    Pt
    LP6960-1
  • System
    Bld/Tiss
    LP7061-7
    • System Core
      Bld/Tiss
      LP7061-7
    • Super System
      NULL
       
  • Scale
    Doc
    LP32888-7
  • Method
    Molgen
    LP6404-0

Basic Attributes

Class
MOLPATH
Type
Laboratory
First Released
Version 2.70
Last Updated
Version 2.70 (ADD)
Order vs. Observation
Both

Language Variants Get Info

TagLanguageTranslation
cs-CZCzech (Czechia)Hereditární karcinom prsu a gynekologický karcinom multigenová analýza:Nález:Časový bod:Krev/tkáň:Dokument:Molekulární genetika
el-GRGreek (Greece)Πολυγονιδιακή ανάλυση κληρονομικού καρκίνου του μαστού και γυναικολογικού καρκίνου:Εύρεση:Pt:Αίμα/Ιστός:Doc:Μοριακή γενετική
Synonyms: Doc MOLPATH Pt Αίμα Αίμα/Ιστός Εύρεση Ιστός Καρκίνος Μοριακή γενετική Πολυγονιδιακή ανάλυση κληρονομικού καρκίνου του μαστού και γυναικολογικού καρκίνου
es-ESSpanish (Spain)Análisis multigénico de cáncer hereditario de mama y ginecológico:Hallazgo:Punto temporal:Sangre o tejido:Doc:Genética molecular
es-MXSpanish (Mexico)Análisis multigénico de cáncer de mama y ginecológico hereditario:Encontrar:Punto temporal:Bld / Tiss:Documento:Molgen
fr-FRFrench (France)Analyse multigénique d'un cancer héréditaire du sein et gynécologique:Recherche:Ponctuel:Sang/Tissu:Document:Biologie moléculaire
it-ITItalian (Italy)Cancro ereditario al seno & ginecologico, analisi multigenica:Osservazione:Pt:Sangue/Tess:Doc:Molgen
Synonyms: Analisi multigenica del cancro ereditario al seno e ginecologico Genetica molecolare Osservazione Patologia molecolare Punto nel tempo (episodio) Sangue Sangue o Tessuto Tessuto & Strisci
pl-PLPolish (Poland)Analiza wielogenowa dziedzicznych nowotworów piersi & narządów płciowych:stwierdzenie:punkt w czasie:krew lub tkanka:dokument:genetyka molekularna
Synonyms: Analiza wielogenowa w kierunku dziedzicznych nowotworów piersi i narządów płciowych diagnostyka molekularna
zh-CNChinese (China)遗传性乳腺癌和妇科癌症多基因分析:发现:时间点:全血/组织:文档型:分子遗传学类实验室方法
Synonyms: 临床文档型;临床文档;文档;文书;医疗文书;临床医疗文书 全血或组织;血液/组织;血液或组织 分子病理学;分子病理学试验 分子遗传学;分子遗传学方法;分子遗传学类方法;分子遗传学类检验方法;包括 RFL、PCR 及其他方法在内，用于在分子基础上检测遗传属性的方法的大类;聚合酶链反应;聚合酶链式反应 发现是一个原子型临床观察指标，并不是作为印象的概括陈述。体格检查、病史、系统检查及其他此类观察指标的属性均为发现。它们的标尺对于编码型发现可能是名义型，而对于叙述型文本之中所报告的发现，则可能是叙述型。;发现物;所见;结果;结论 时刻;随机;随意;瞬间 未作说明的组织;组织;组织 & 涂片 癌 血;血液 遗传性乳腺癌和妇科癌症（妇科癌）多基因分析

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

CodeSystem lookup
https://fhir.loinc.org/CodeSystem/$lookup?system=http://loinc.org&code=97655-5